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2-Phenoxyethyl chloride

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2-Phenoxyethyl chloride manufacturers

2-Phenoxyethyl chloride Basic information
Product Name:2-Phenoxyethyl chloride
Synonyms:(2-chloroethoxy)-benzen;1-Phenoxy-2-chloroethane;benzene,(2-chloroethoxy);benzene,(2-chloroethoxy)-;beta-Phenoxyethyl chloride;-Chlorophenetole;Ether, 2-chloroethyl phenyl;Phenetole, beta-chloro-
CAS:622-86-6
MF:C8H9ClO
MW:156.61
EINECS:210-757-0
Product Categories:Pharmaceutical Intermediates;Phenetole;Aromatics Compounds;Aromatics
Mol File:622-86-6.mol
2-Phenoxyethyl chloride Structure
2-Phenoxyethyl chloride Chemical Properties
Melting point 28°C
Boiling point 97-98 °C15 mm Hg(lit.)
density 1.129 g/mL at 25 °C(lit.)
refractive index n20/D 1.534(lit.)
Fp 213 °F
storage temp. under inert gas (nitrogen or Argon) at 2-8°C
solubility Chloroform, Ethyl Acetate
form Solid
color Pale Yellow Oil to Low Melting Colorless
BRN 971048
InChI1S/C8H9ClO/c9-6-7-10-8-4-2-1-3-5-8/h1-5H,6-7H2
InChIKeyVQUYNUJARXBNPK-UHFFFAOYSA-N
SMILESClCCOc1ccccc1
CAS DataBase Reference622-86-6(CAS DataBase Reference)
NIST Chemistry ReferenceBenzene, (2-chloroethoxy)-(622-86-6)
EPA Substance Registry System(2-Chloroethoxy)benzene (622-86-6)
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 26-36
RIDADR UN 3265
WGK Germany 3
F 10-21
TSCA TSCA listed
HS Code 29093090
Storage Class10 - Combustible liquids
Hazard ClassificationsEye Irrit. 2
Skin Irrit. 2
STOT SE 3
MSDS Information
ProviderLanguage
SigmaAldrich English
ALFA English
2-Phenoxyethyl chloride Usage And Synthesis
Chemical PropertiesPale Yellow Oil
UsesPhenyl 2-Chloroethyl Ether (cas# 622-86-6) is a compound useful in organic synthesis.
Uses(2-Chloroethoxy)benzene is used in the coupling reaction of benzaldehyde, cinnamyltrimethylsilane and anisole in the synthesis of pseudo-symmetrical tamoxifen derivatives.
Synthesis
2-Phenoxyethanol

122-99-6

2-Phenoxyethyl chloride

622-86-6

At room temperature, 2.5 mL of N-methylpyrrolidone (NMP), 1.38 g (10 mmol) of 2-phenoxyethanol and 1.5 mL (11 mmol) of benzenesulfonyl chloride were added to the reaction flask. The mixture was stirred well and then the reaction was continuously stirred at 100 °C for 30 min. Upon completion of the reaction, the reaction mixture was cooled to room temperature and subsequently extracted by adding 30 mL of dichloromethane and 30 mL of water. The organic layer was separated and washed with saturated brine and dried over anhydrous sodium sulfate. Dichloromethane was removed by evaporation under reduced pressure to give the crude product. The crude product was purified by column chromatography to give 1.52 g of 2-chlorophenetole in colorless liquid form in 96.8% yield.

References[1] Patent: CN106187674, 2016, A. Location in patent: Paragraph 0017; 0018
[2] Patent: US2016/347717, 2016, A1. Location in patent: Paragraph 0232; 0233
[3] Patent: US5527816, 1996, A
[4] Chemical Research in Toxicology, 2000, vol. 13, # 1, p. 53 - 62
[5] Patent: CN106146450, 2016, A. Location in patent: Paragraph 0132; 0133; 0134
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