GB609803A - A process for the preparation of 2-methyl-2.3-di-halogen-tetrahydrofuranes and their conversion to vitamin b and the like - Google Patents

A process for the preparation of 2-methyl-2.3-di-halogen-tetrahydrofuranes and their conversion to vitamin b and the like

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Publication number
GB609803A
GB609803A GB4543/41A GB454341A GB609803A GB 609803 A GB609803 A GB 609803A GB 4543/41 A GB4543/41 A GB 4543/41A GB 454341 A GB454341 A GB 454341A GB 609803 A GB609803 A GB 609803A
Authority
GB
United Kingdom
Prior art keywords
aceto
halogen
vitamin
methyl
preparation
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired
Application number
GB4543/41A
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Chinoin Private Co Ltd
Original Assignee
Chinoin Gyogyszer es Vegyeszeti Termekek Gyara Zrt
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Chinoin Gyogyszer es Vegyeszeti Termekek Gyara Zrt filed Critical Chinoin Gyogyszer es Vegyeszeti Termekek Gyara Zrt
Publication of GB609803A publication Critical patent/GB609803A/en
Expired legal-status Critical Current

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Abstract

Vitamin B1 is obtained by reacting, preferably in the presence of acid binding agents, 2-alkyl-4-amino - 5 - (thioformamido - alkyl) pyrimidines with 2-methyl-2 : 3-dihalogen-tetrahydrofuranes prepared by subjecting g - aceto - g - halogen - propyl alcohol, or its cyclic form, or an ether of the cyclic form such as an alkyl ether or its ether formed with g -aceto-g -halogen-propyl alcohol, or mixtures of them, or reaction mixtures containing any one of these compounds, to reagents which are generally used for substituting a hydroxyl by a halogen group. Preferably, the reaction is carried out in 90 per cent formic acid as the reaction medium. Suitable acid binding agents are pyridine and potassium formate. Detailed examples are given of the preparation of 2-methyl-2 : 3-dichloro-tetrahydrofurane by treating aceto-chloro-propyl alcohol with an aceto-chlorobutyrolactone with thionyl chloride, hydrogen chloride gas and hydrochloric acid. An additional example describes the preparation of Vitamin B1 using pyridine as the acid binding agent.
GB4543/41A 1940-05-25 1941-04-04 A process for the preparation of 2-methyl-2.3-di-halogen-tetrahydrofuranes and their conversion to vitamin b and the like Expired GB609803A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
HU609803X 1940-05-25

Publications (1)

Publication Number Publication Date
GB609803A true GB609803A (en) 1948-10-07

Family

ID=10979734

Family Applications (1)

Application Number Title Priority Date Filing Date
GB4543/41A Expired GB609803A (en) 1940-05-25 1941-04-04 A process for the preparation of 2-methyl-2.3-di-halogen-tetrahydrofuranes and their conversion to vitamin b and the like

Country Status (1)

Country Link
GB (1) GB609803A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2678319A (en) * 1952-02-20 1954-05-11 Du Pont Preparation of 2,3-dihalotetrahydro-2-methylfurans

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2678319A (en) * 1952-02-20 1954-05-11 Du Pont Preparation of 2,3-dihalotetrahydro-2-methylfurans

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