Basic information Safety Supplier Related
ChemicalBook >  Product Catalog >  Organic Chemistry >  Amides >  1-[(AMMONIOOXY)METHYL]-4-CHLOROBENZENE CHLORIDE

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

Basic information Safety Supplier Related

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

Product Name:
1-[(AMMONIOOXY)METHYL]-4-CHLOROBENZENE CHLORIDE
Synonyms:
  • 1-[(aminooxy)methyl]-4-chlorobenzene hydrochloride (1:1)
  • o-(p-chlorobenzyl)-hydroxylaminhydrochloride
  • O-(4-CHLOROBENZYL)HYDROXYLAMINE HYDROCHLORIDE
  • 1-[(AMINOOXY)METHYL]-4-CHLOROBENZENE HYDROCHLORIDE
  • 1-[(AMMONIOOXY)METHYL]-4-CHLOROBENZENE CHLORIDE
  • O-(4-chlorobenzyl) hydroxylaMine
  • 4-Chlorobenzyloxyamine hydrochloride
  • O-(4-Chlorobenzyl)hydroxylamine hydrochloride 4-Chlorobenzyloxyamine hydrochloride
CAS:
38936-60-6
MF:
C7H9Cl2NO
MW:
194.06
Mol File:
38936-60-6.mol
More
Less

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

Melting point:
230°C
form 
solid
color 
White
More
Less

Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36/37/39
HazardClass 
IRRITANT
HS Code 
2921199990
More
Less

1-[(AMMONIOOXY)METHYL]-4-CHLOROBENZENE CHLORIDE Usage And Synthesis

Preparation

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.

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

J & K SCIENTIFIC LTD.
Tel
010-82848833 400-666-7788
Email
jkinfo@jkchemical.com
Meryer (Shanghai) Chemical Technology Co., Ltd.
Tel
021-61259108 18621169109
Email
market03@meryer.com
Wuhan Chemwish Technology Co., Ltd
Tel
86-027-67849912
Email
sales@chemwish.com
XiaoGan ShenYuan ChemPharm co,ltd
Tel
15527768850
Email
1791901229@qq.com
TaiZhou ZhiCheng Chemicals & Technology Co., LTD.
Tel
0523-82837785 13914525028
Email
info@jszchg.com