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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 461738Generated: October 30, 2026

Thionyl Chloride → HCID 70637434, compound

https://huagongshe.com/reaction/461738

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
ReactantHCID 70637620HCID 70637620—
SolventBenzeneHCID 241—
ProductHCID 70637434HCID 70637434—

Reaction Steps

A mixture of 14.7 parts of 3-(1-hydroxyethyl)-o-tolyl 2-thienyl ketone and 126 parts of benzene is stirred while cooling on an ice-bath. Then 9.5 parts of thionyl chloride are added and the whole is stirred further over week-end at room temperature. The reaction mixture is evaporated in vacuo, yielding 3-(1-chloroethyl)-o-tolyl 2-thienyl ketone as a residue.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04064132
Source datasetuspto-grants-1977_12
ORD IDord-a41ef484ee9a49528a416df6799ae2ec
Source noteuspto-grants-1977_12