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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1403682Generated: October 30, 2026

tert-Butyl chloroacetate → tert-Butyl [(ethoxycarbonothioyl)sulfanyl]acetate

https://huagongshe.com/reaction/1403682

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl chloroacetateHCID 66052—
ReactantPotassium ethylxanthateHCID 2735045—
SolventAcetoneHCID 180—
Producttert-Butyl [(ethoxycarbonothioyl)sulfanyl]acetateHCID 10857462102%

Reaction Steps

Potassium ethylxanthate (58.0 g, 364 mmol) was suspended in 200 mL of dry acetone at room temperature. tert-Butyl chloroacetate (50 g, 332 mmol) was added dropwise with stirring. After 18 hrs potassium chloride was removed by fitration, and the solvent was evaporated. The residue was taken up into ether, washed with 5% NaHCO3, water, and brine, dried over MgSO4, filtered, and evaporated to leave 80 g of O-ethyl S-(tert-butoxycarbonyl)methyl dithiocarbonate as a thick oil. This oil was stirred with ethanolamine (323 mmol) for 2 hrs at room temperature. The reaction mixture was taken up into ethyl acetate, washed with 1.2N HCl, water, and brine, dried over MgSO4, filtered, and evaporated. The residue was vacuum dis-tilled to give 30 g of mercapto-acetic acid tert-butyl ester as a clear oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08912209B2
Source datasetuspto-grants-2014_12
ORD IDord-536a5b04256d4188a8c35f515881cccb
Source noteuspto-grants-2014_12