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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2076692Generated: October 31, 2026

Thionyl Chloride → HCID 67119342, compound

https://huagongshe.com/reaction/2076692

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
ReactantHCID 67119374HCID 67119374—
SolventDichloromethaneHCID 6344—
ProductHCID 67119342HCID 6711934271%

Reaction Steps

After thionyl chloride (4 ml) was added to a solution of (2-ethyl-4′-methoxy-1,1′-biphenyl-3-yl)methanol (4.39 g, 17.9 mmol) obtained in Example (90-3) in methylene chloride (18 ml) under ice-cooling, the mixture was stirred at room temperature for 7 hours. The residue obtained by removing the solvent under reduced pressure was diluted with ethyl acetate and the mixture was successively washed with water, a saturated aqueous sodium hydrogencarbonate solution and a saturated aqueous NaCl solution and dried with anhydrous sodium sulfate. The solvent was removed under reduced pressure to give 3′-(chloromethyl)-2′-ethyl-1,1′-biphenyl-4-yl methyl ether (3.32 g, yield: 71%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07923573B2
Source datasetuspto-grants-2011_04
ORD IDord-130fbbe17d4943a09237778bbd7a064f
Source noteuspto-grants-2011_04