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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 65518Generated: October 25, 2026

Ethanethiol → 4-bromo-3-oxothiobutyric acid-S-ethyl ester

https://huagongshe.com/reaction/65518

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanethiolHCID 6343—
ReactantPropylene OxideHCID 6378—
ReactantDiketeneHCID 12661—
ReactantBromineHCID 24408—
ReactantSodium BicarbonateHCID 516892—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product4-bromo-3-oxothiobutyric acid-S-ethyl esterHCID 1382165758.2%

Reaction Conditions

Temperature-40 °C

Reaction Steps

In 40 ml of anhydrous methylene chloride was dissolved 8.4 g of diketene, and the resulting solution was cooled to -40° C. Then, 14.4 g of bromine was added dropwise to the solution while maintaining the temperature at -40° to -35° C. over a period of 1 hour, and the resulting mixture was subjected to reaction at -30° to -20° C. for 30 minutes. On the other hand, 7.48 g of ethanethiol and 5.84 g of propylene oxide were dissolved in 60 ml of anhydrous methylene chloride, and the resulting solution was cooled to -40° C. Into this solution was introduced the above-mentioned reaction mixture. Then, the temperature of the reaction mixture was raised up to room temperature over a period of 1 hour, and the mixture was further subjected to reaction at the same temperature for 1 hour. The reaction mixture was introduced into 100 ml of water at 5° C., and the pH was adjusted to 6.0 with sodium hydrogencarbonate. The organic layer was separated, washed with 30 ml of saturated aqueous sodium chloride solution and then dried over anhydrous magnesium sulfate. The solvent was removed by distillation under reduced pressure and the residue obtained was distilled under reduced pressure to obtain 11.8 g (yield, 58.0%) of 4-bromo-3-oxothiobutyric acid-S-ethyl ester having a boiling point of 110°-120° C./4 mmHg.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04614819
Source datasetuspto-grants-1986_09
ORD IDord-717b35c4eb894f3b96a55ccdf92a5903
Source noteuspto-grants-1986_09