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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1909521Generated: October 29, 2026

Thionyl Chloride → HCID 58566473, compound

https://huagongshe.com/reaction/1909521

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
ReactantHCID 58566649HCID 58566649—
SolventDichloromethaneHCID 6344—
ProductHCID 58566473HCID 5856647367%

Reaction Steps

Thionyl chloride (0.415 mL, 5.69 mmol) was added slowly to an ice cold solution of the alcohol (510) (0.203 g, 1.14 mmol) in dichloromethane (6.0 mL). The reaction mixture was stirred and warmed to room temperature for 1 h. The resulting solution was quenched slowly with saturated sodium bicarbonate (10 mL) and extracted with dichloromethane, the organic layer was dried over sodium sulfate, filtered, and concentrated in vacuo to provide the intermediate 7-(chloromethyl)-2-methylbenzo[b]thiophene (511) (0.150 g, 67.0%) as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08598374B2
Source datasetuspto-grants-2013_12
ORD IDord-45eb69f456ab4a11aea34defb0814329
Source noteuspto-grants-2013_12