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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1666494Generated: October 30, 2026

Thionyl Chloride → HCID 66876006, compound

https://huagongshe.com/reaction/1666494

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 66875762HCID 66875762—
SolventDichloromethaneHCID 6344—
ProductHCID 66876006HCID 6687600699.9%

Reaction Steps

[3-(4-Methyl-pyridin-2-yloxy)-phenyl]-methanol from Step 1 (4.75 g, 22.1 mmol), in dichloromethane (50 mL), was cooled to 0° C., and treated dropwise with thionyl chloride (1.93 mL, 26.5 mmol). The reaction mixture was allowed to warm to ambient temperature and was stirred for 3 h. Saturated aqueous sodium bicarbonate (20 mL) was added and the mixture was stirred at rt for 5 min. The organic layer was separated, dried over sodium sulfate, filtered and concentrated by evaporation to afford the desired product (5.16 g, 99% yield) as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08044052B2
Source datasetuspto-grants-2011_10
ORD IDord-45f6cd7ced714848b4d99ed0c13b1bdf
Source noteuspto-grants-2011_10