+++1 Chemisches Zentralblatt
+++1 Chemisches Zentralblatt
Добрый день, помогите пожалуйста с рефератом, т.к. не могу найти оригинал - Итал. Пат. 626063 (1964)
Chemisches Zentralblatt 1966, Bd. 137, 2486.
Chemisches Zentralblatt 1966, Bd. 137, 2486.
Последний раз редактировалось SergSam Пн сен 05, 2011 12:27 pm, всего редактировалось 1 раз.
Re: 1 Chemisches Zentralblatt
НАдо глядеть у нас
"Ничто так не воодушевляет, как осознание своего безнадежного положения." Альбер Камю.
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Arkadii_Tarasevych
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Re: 1 Chemisches Zentralblatt
Я нашёл у себя в библиотеке, только ни сканера, ни фотоаппарата сейчас нет. Попробую отдолжить и сфотографировать на днях. Там есть ссылка, как я понял, на первоначальный британский патент 1960 года. Может он где в инете есть?!
Brit Pat 964097 30/12/1960.
Brit Pat 964097 30/12/1960.
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Arkadii_Tarasevych
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Re: 1 Chemisches Zentralblatt
Вот я недолго поискал и нашёл кое-что:
Process of preparing a carboxylic acid derivative
Page bookmark GB 964097 (A) - Process of preparing a carboxylic acid derivative
Publication date: 1964-07-15
Inventor(s):
Applicant(s): MONTEDISON SPA + (MONTECATINI SOCIETA GENERALE PER L'INDUSTRIA MINERARIA E CHIMICA)
Classification: - international: B01J23/70; C07C51/31; C07C51/353
- European: C07C121/40F; C07C51/353; C07C51/31; C07C51/31
Application number: GB19600044787 19601230
Priority number(s): IT19590021846 19591231; IT19600000845 19600118
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Also published as: DE 1254141 (B)
Abstract of GB 964097 (A)
Translate this text
Carboxylic acid derivatives are obtained by treating an aliphatic or alicyclic ketone peroxide with acrylonitrile or an acrylic ester of a C1- 5 alkanol and HCl or HBr in the presence of ferrous or cuprous ions, e.g. at -10 DEG C. to + 10 DEG C. The ketone peroxides are generally formulated as 1-hydroxy-hydroperoxides. The two types of reaction involved are: <FORM:0964097/C1/1> and <FORM:0964097/C1/2> where R1 is CN or COOR (R being C1- 5 alkyl) and R1 and R2 are e.g. alkyl groups; and the corresponding reactions with HBr and with other alicyclic ketone peroxides. In examples, (1), (11) cyclopentanone peroxide, acrylonitrile and HCl give HOOC(CH2)5CHClCN, which is hydrolysed and esterified to CH3OOC(CH2)5CHClCOOCH3 this is hydrolysed to the free acid, and the latter hydrogenated to suberic acid; (2), (3) and (7) methyl ethyl ketone or diethyl ketone peroxide, acrylonitrile and HCl give a -chlorovaleronitrile, which is hydrolysed to a -chlorovaleric acid; (4) methyl hexyl ketone peroxide, acrylonitrile and HCl give a product which is hydrolysed to a -chlorononanoic acid; (5) methyl heptyl ketone peroxide, acrylonitrile and HCl similarly give a -chlorodecanoic acid; (6) methyl ethyl ketone peroxide, acrylonitrile and HBr similarly give a -bromovaleric acid; (8) methyl ethyl ketone peroxide, methyl acrylate and HCl give methyl a -chlorovalerate; (9) cyclohexanone peroxide, treated as in (1), gives successively HOOC(CH2)6 CHClCN and CH3OOC(CH2)6CHClCOOCH3; (10) cyclohexanone peroxide, butyl acrylate and HCl gives the butyl ester of a -chloroazelaic acid; (12) Methyl a -chloroazelate is hydrolysed and hydrogenated to produce azelaic acid. Specifications 884,761 and 890,141 are referred to.
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Код: Выделить всё
http://worldwide.espacenet.com/publicationDetails/biblio?DB=EPODOC&II=9&adjacent=true&locale=en_EP&FT=D&date=19640715&CC=GB&NR=964097A&KC=APage bookmark GB 964097 (A) - Process of preparing a carboxylic acid derivative
Publication date: 1964-07-15
Inventor(s):
Applicant(s): MONTEDISON SPA + (MONTECATINI SOCIETA GENERALE PER L'INDUSTRIA MINERARIA E CHIMICA)
Classification: - international: B01J23/70; C07C51/31; C07C51/353
- European: C07C121/40F; C07C51/353; C07C51/31; C07C51/31
Application number: GB19600044787 19601230
Priority number(s): IT19590021846 19591231; IT19600000845 19600118
View INPADOC patent family
View list of citing documents
Also published as: DE 1254141 (B)
Abstract of GB 964097 (A)
Translate this text
Carboxylic acid derivatives are obtained by treating an aliphatic or alicyclic ketone peroxide with acrylonitrile or an acrylic ester of a C1- 5 alkanol and HCl or HBr in the presence of ferrous or cuprous ions, e.g. at -10 DEG C. to + 10 DEG C. The ketone peroxides are generally formulated as 1-hydroxy-hydroperoxides. The two types of reaction involved are: <FORM:0964097/C1/1> and <FORM:0964097/C1/2> where R1 is CN or COOR (R being C1- 5 alkyl) and R1 and R2 are e.g. alkyl groups; and the corresponding reactions with HBr and with other alicyclic ketone peroxides. In examples, (1), (11) cyclopentanone peroxide, acrylonitrile and HCl give HOOC(CH2)5CHClCN, which is hydrolysed and esterified to CH3OOC(CH2)5CHClCOOCH3 this is hydrolysed to the free acid, and the latter hydrogenated to suberic acid; (2), (3) and (7) methyl ethyl ketone or diethyl ketone peroxide, acrylonitrile and HCl give a -chlorovaleronitrile, which is hydrolysed to a -chlorovaleric acid; (4) methyl hexyl ketone peroxide, acrylonitrile and HCl give a product which is hydrolysed to a -chlorononanoic acid; (5) methyl heptyl ketone peroxide, acrylonitrile and HCl similarly give a -chlorodecanoic acid; (6) methyl ethyl ketone peroxide, acrylonitrile and HBr similarly give a -bromovaleric acid; (8) methyl ethyl ketone peroxide, methyl acrylate and HCl give methyl a -chlorovalerate; (9) cyclohexanone peroxide, treated as in (1), gives successively HOOC(CH2)6 CHClCN and CH3OOC(CH2)6CHClCOOCH3; (10) cyclohexanone peroxide, butyl acrylate and HCl gives the butyl ester of a -chloroazelaic acid; (12) Methyl a -chloroazelate is hydrolysed and hydrogenated to produce azelaic acid. Specifications 884,761 and 890,141 are referred to.
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Arkadii_Tarasevych
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Re: 1 Chemisches Zentralblatt
Тот же патент, только на немецком. Это то что нужно?
У вас нет необходимых прав для просмотра вложений в этом сообщении.
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Arkadii_Tarasevych
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Re: 1 Chemisches Zentralblatt
Да, судя по абстракту из Chem Zentralblatt это - то же изобретение.
Re: 1 Chemisches Zentralblatt
Огромное спасибо!!! Да, это оно
Очень благодарен за Ваш труд
Очень благодарен за Ваш труд
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Arkadii_Tarasevych
- Сообщения: 635
- Зарегистрирован: Пн фев 08, 2010 11:15 pm
Re: +++1 Chemisches Zentralblatt
Пожалуйста!:)
Кто сейчас на конференции
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