JPS577461A - Production of oxime - Google Patents

Production of oxime

Info

Publication number
JPS577461A
JPS577461A JP8194580A JP8194580A JPS577461A JP S577461 A JPS577461 A JP S577461A JP 8194580 A JP8194580 A JP 8194580A JP 8194580 A JP8194580 A JP 8194580A JP S577461 A JPS577461 A JP S577461A
Authority
JP
Japan
Prior art keywords
hypohalite
aldehyde
amount
reaction
formula
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.)
Pending
Application number
JP8194580A
Other languages
Japanese (ja)
Inventor
Tetsuyoshi Suzuki
Sunao Imaki
Tameichi Ochiai
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.)
Mitsubishi Kasei Corp
Original Assignee
Mitsubishi Kasei Corp
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 Mitsubishi Kasei Corp filed Critical Mitsubishi Kasei Corp
Priority to JP8194580A priority Critical patent/JPS577461A/en
Publication of JPS577461A publication Critical patent/JPS577461A/en
Pending legal-status Critical Current

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  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

PURPOSE: The reaction of a hypohalite with aldehyde and hydroxylamine salt gives the titled compound that is used to produce an insecticide in one-stage by no use of a large amount of base.
CONSTITUTION: A hypohalite salt is made to act on an aldehyde of formula I (R is lower alkyl) such as acetaldehyde and a hydroxylamine salt such as hydroxylamine hydrochloride to give the titled compound of formula II (X is halogen). The example of the hypohalite is sodium hypochlorite and the amount is usually 0.5W2.0mol, preferably 0.8W1.2mol/mol of the aldehyde. When the amount of the hypochlorite used is too small, the reaction does not proceed sufficiently, whereas an excessive amount undesirably causes the halogenation and oxidation of the objective product. Since the hypohalite plays roles of both neutralizer and halogenating agent in the conventional process, a large amount of base becomes unnecessary.
COPYRIGHT: (C)1982,JPO&Japio
JP8194580A 1980-06-17 1980-06-17 Production of oxime Pending JPS577461A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP8194580A JPS577461A (en) 1980-06-17 1980-06-17 Production of oxime

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP8194580A JPS577461A (en) 1980-06-17 1980-06-17 Production of oxime

Publications (1)

Publication Number Publication Date
JPS577461A true JPS577461A (en) 1982-01-14

Family

ID=13760634

Family Applications (1)

Application Number Title Priority Date Filing Date
JP8194580A Pending JPS577461A (en) 1980-06-17 1980-06-17 Production of oxime

Country Status (1)

Country Link
JP (1) JPS577461A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH03116634A (en) * 1989-09-28 1991-05-17 Nec Corp Microwave tube
CN114478338A (en) * 2022-02-07 2022-05-13 浙江锦华新材料股份有限公司 Preparation method of high-purity alpha-methylthio acetyl oxime

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH03116634A (en) * 1989-09-28 1991-05-17 Nec Corp Microwave tube
CN114478338A (en) * 2022-02-07 2022-05-13 浙江锦华新材料股份有限公司 Preparation method of high-purity alpha-methylthio acetyl oxime
CN114478338B (en) * 2022-02-07 2024-04-30 浙江锦华新材料股份有限公司 Preparation method of high-purity alpha-methylthio acetoxime

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