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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 329446Generated: October 30, 2026

Bromine → HCID 13784978, compound

https://huagongshe.com/reaction/329446

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromineHCID 24408—
ReactantMethyl [2-(phenylsulfanyl)-5-propanoylphenyl]acetateHCID 14279620—
ReactantHCID 18364422HCID 18364422—
ReactantMethylorthoformateHCID 53629101—
CatalystZinc bromideHCID 10421208—
SolventMethanolHCID 887—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 13784978HCID 1378497880%

Reaction Steps

To a stirred mixture of 15.72 g (50 mmol.) of methyl 5-propionyl-2-phenylthiophenylacetate, 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 13.78 g of the desired product as a yellow oil (yield 80%, b.p. 212°-215° C./2 mmHg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04891433
Source datasetuspto-grants-1990_01
ORD IDord-1b8d2aa8c20148fcb22f0bbd3a5d56f5
Source noteuspto-grants-1990_01