1-[(AMMONIOOXY)METHYL]-4-CHLOROBENZENE CHLORIDE

1-[(AMMONIOOXY)METHYL]-4-CHLOROBENZENE CHLORIDE 구조식 이미지
카스 번호:
38936-60-6
상품명:
1-[(AMMONIOOXY)METHYL]-4-CHLOROBENZENE CHLORIDE
동의어(영문):
O-(4-chlorobenzyl) hydroxylaMine;O-(4-CHLOROBENZYL)HYDROXYLAMINE HCL;4-Chlorobenzyloxyamine hydrochloride;o-(p-chlorobenzyl)-hydroxylaminhydrochloride;O-(p-Chlorobenzyl)hydroxylamine hydrochloride;O-(4-CHLOROBENZYL)HYDROXYLAMINE HYDROCHLORIDE;1-[(AMMONIOOXY)METHYL]-4-CHLOROBENZENE CHLORIDE;1-[(AMINOOXY)METHYL]-4-CHLOROBENZENE HYDROCHLORIDE;O-[(4-chlorophenyl)methyl]Hydroxylamine hydrochloride;1-[(aminooxy)methyl]-4-chlorobenzene hydrochloride (1:1)
CBNumber:
CB9734432
분자식:
C7H9Cl2NO
포뮬러 무게:
194.06
MOL 파일:
38936-60-6.mol

1-[(AMMONIOOXY)METHYL]-4-CHLOROBENZENE CHLORIDE 속성

녹는점
230°C
물리적 상태
고체
물리적 상태
단단한 모양
색상
하얀색

안전

위험품 표기 Xi
위험 카페고리 넘버 36/37/38
안전지침서 26-36/37/39
위험 등급 IRRITANT
HS 번호 2921199990

1-[(AMMONIOOXY)METHYL]-4-CHLOROBENZENE CHLORIDE C화학적 특성, 용도, 생산

제조 방법

To a solution of 83.7 gm (1.5 moles) of potassium hydroxide in 560 ml of water is added in turn with stirring, 300 gm (0.985 mole) of dipotassium hydroxylaminedisulfonate and 161 gm (1.0 mole) of 4-chlorobenzyl chlo­ride. The stirred mixture is heated on a steam bath for 1.75 hr. After cool­ing, the precipitate is filtered off and refluxed for 3 hr in 1000 ml of 1.5 Ν sulfuric acid. The reaction mixture is then cooled and made strongly alkaline with a 15% aqueous sodium hydroxide solution. The mixture is then extracted with ether repeatedly. The ether extracts are combined and evaporated to dryness. The solid residue (crude free base, 80 gm, i.e., 51.5% of theory, m.p. 35-38°C) is taken up in 1 liter of ether. Anhydrous hydrogen chloride is bubbled through this solution to precipitate the hy­drochloride salt. The yield is 59 gm (31%, overall), m.p. 243-244°C (dec); the free base has b.p. 100°C/1 mm Hg. In this preparation, the hydrolysis of the alkylated dipotassium hydroxyl­aminedisulfonate with only 1 liter of 1.5 Ν sulfuric acid seems somewhat skimpy. We suggest that a higher level of sulfuric acid be considered at that stage of the reaction, if the alkylation has indeed gone to completion. Once the O-alkylhydroxylamine has been prepared by this reaction, it may be N-alkylated to produce an N,Ο-dialkylhydroxylamine.
The preparation of O-phenylhydroxylamine has been a synthetic chal­lenge for some time since it is quite unstable. Using hydroxylamine-O-sulfonic acid. A small quantity of this compound has been prepared [36]. Reaction conditions probably require further study to improve the yield. Extension of the reaction to the preparation of O-alkylhydroxylamines would be of interest. Preparation of O-(4-Chlorobenzyl)hydroxylamine hydrochloride

1-[(AMMONIOOXY)METHYL]-4-CHLOROBENZENE CHLORIDE 준비 용품 및 원자재

원자재

준비 용품


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