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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1704023Generated: October 27, 2026

p-Chlorothiophenol → Methyl alpha-(p-chlorophenylthio)-alpha-[p-(p-chlorophenoxy)phenyl]acetate

https://huagongshe.com/reaction/1704023

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-ChlorothiophenolHCID 7815—
ReactantMethyl alpha-Bromo-alpha-[p-(p-chlorophenoxy)phenyl]acetateHCID 20392594—
SolventMethanolHCID 887—
ProductMethyl alpha-(p-chlorophenylthio)-alpha-[p-(p-chlorophenoxy)phenyl]acetateHCID 20392626—

Reaction Steps

Methyl α-bromo-α-[p-(p-chlorophenoxy)phenyl]acetate (7.11 g) is reacted with 3.61 g of 4-chlorothiophenol in methanol, as in Example 16, to give a yellow oil which is bulb distilled at 0.01 mm to afford colorless oil (188° C) which solidifies to give white crystals, mp 71°-75° C. A portion is recrystallized from hexane to give white nedles, mp 74°-75.5° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04125729
Source datasetuspto-grants-1978_11
ORD IDord-86ad3fe8552b4dd88975487d13014ed0
Source noteuspto-grants-1978_11