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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 329447Generated: October 28, 2026

Bromine → HCID 13784978, compound

https://huagongshe.com/reaction/329447

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromineHCID 24408—
Reactant[2-(Phenylsulfanyl)-5-propanoylphenyl]acetic acidHCID 13650250—
ReactantHCID 18364422HCID 18364422—
ReactantMethylorthoformateHCID 53629101—
CatalystZinc bromideHCID 10421208—
SolventMethanolHCID 887—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 13784978HCID 1378497870%

Reaction Steps

To a stirred mixture of 15.0 g (50 mmol.) of 5-propionyl-2-phenylthiophenylacetic acid, 13.32 g (125.5 mmol.) of methyl orthoformate, 20 ml of methanol and 20 ml ethylene tetrachloride was dropwise added under stirring 8.39 g (52.5 mmol.) of bromine for a period of 30 minutes. The resulting mixture was further stirred at room temperature for 30 minutes, and then was heated slowly to 110° C. for 1 hour, under distilling off materials having a low boiling point. To the reaction mixture was added 0.90 g (4.0 mmol.) of zinc bromide, and the mixture was heated to 110° C. under reflux for 3 hours. The reaction mixture was cooled, and 75 ml of water and 40 ml of methylene chloride were added. The organic layer was separated and the solvent was distilled off under reduced pressure. The residue was distilled under reduced pressure to obtain 12.1 g of the desired product as a yellow oil (yield 70%, b.p. 212°-215° C./2 mmHg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04891433
Source datasetuspto-grants-1990_01
ORD IDord-c0047ad32fb7421c8e5f78adcf497932
Source noteuspto-grants-1990_01