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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | tert-Butyl chloroacetate | HCID 66052 | — |
| Reactant | Potassium ethylxanthate | HCID 2735045 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | tert-Butyl [(ethoxycarbonothioyl)sulfanyl]acetate | HCID 10857462 | 102% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08912209B2 |
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| Source dataset | uspto-grants-2014_12 |
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| ORD ID | ord-536a5b04256d4188a8c35f515881cccb |
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| Source note | uspto-grants-2014_12 |
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