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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 253477Generated: October 30, 2026

Thionyl Chloride → HCID 178488083, compound

https://huagongshe.com/reaction/253477

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
ReactantHCID 178488091HCID 178488091—
SolventDichloromethaneHCID 6344—
ProductHCID 178488083HCID 178488083—

Reaction Steps

(5-Methoxy-1H-benzoimidazol-2-yl)-methanol (221, 0.5 g, 3 mmol) was combined with 30 mL dichloromethane. Thionyl chloride (0.51 mL, 7 mmol) was added and the reaction was stirred at room temperature for 2 hours. The reaction was concentrated. Ethyl acetate was added and washed with sodium bicarbonate saturated solution and brine. The organic portion was dried over anhydrous sodium sulfate, filtered through Celite and evaporated to dryness. The resulting desired compound was used without further purification. MS (ESI) [M+H+]+=197.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07872018B2
Source datasetuspto-grants-2011_01
ORD IDord-efff9778628f49d1b04981788b941817
Source noteuspto-grants-2011_01