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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1863278Generated: November 2, 2026

Thiophenol → Methyl alpha-(phenylthio)-alpha-[p-(p-chlorophenoxy)phenyl]acetate

https://huagongshe.com/reaction/1863278

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThiophenolHCID 7969—
ReactantMethyl alpha-Bromo-alpha-[p-(p-chlorophenoxy)phenyl]acetateHCID 20392594—
SolventMethanolHCID 887—
ProductMethyl alpha-(phenylthio)-alpha-[p-(p-chlorophenoxy)phenyl]acetateHCID 20392614—

Reaction Steps

Methyl α-bromo-α-[p-(p-chlorophenoxy)phenyl]acetate (7.11 g) is reacted with 2.75 g of thiophenol in methanol, as in Example 16, to yield a yellow oil. After a brief distillation at 0.02 mm to remove volatile impurities, the residue is evaporatively distilled (173° C. @ 0.01 mm) to afford the product as a colorless oil which solidifies, mp 64°-68.5° C. A portion is recrystallized from hexane to give white plates, mp 71.5°-72.5° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04168385
Source datasetuspto-grants-1979_09
ORD IDord-1c5e0e1bba104607a7eb3350d59f7455
Source noteuspto-grants-1979_09