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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1458537Generated: November 3, 2026

Thionyl Chloride → HCID 13948363, compound

https://huagongshe.com/reaction/1458537

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
ReactantSodium BicarbonateHCID 516892—
ReactantEthyl 3-hydroxy-2-phenylpropanoateHCID 596249—
SolventDichloromethaneHCID 6344—
ProductHCID 13948363HCID 1394836345.6%

Reaction Steps

To ethyl 3-hydroxy-2-phenylpropionate (2.55 g, 13.1 mmol) in dichloromethane (15 ml), SOCl2 (1.87 g, 15.7 mmol) in dichloromethane (1 ml) was added while chilling with ice. After the resulting solution was stirred to cause reaction at room temperature for 3 hours, saturated aqueous sodium bicarbonate was added while chilling with ice. The prepared solution was extracted with dichloromethane, and the extract was washed with saturated aqueous sodium chloride, and then dried over anhydrous sodium sulfate. Subsequently, the solvent was removed by distillation under reduced pressure to obtain a crude product. The product was purified by silica gel column chromatography using acetone/hexane=1/3 to obtain 1.27 g of the titled compound as a colorless oil (yield: 45.5%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05852006
Source datasetuspto-grants-1998_12
ORD IDord-0217eb779eb64be4bb10f3b942e172bb
Source noteuspto-grants-1998_12