HuagongsheHuagongshe Chemistry Print Report · For research reference only
Chlorotrimethylsilane → Ethyl [(trimethylsilyl)sulfanyl]acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Chlorotrimethylsilane | HCID 6397 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethyl Thioglycolate | HCID 12185 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | Ethyl [(trimethylsilyl)sulfanyl]acetate | HCID 13310493 | 68.1% |
Reaction Steps
To a solution of ethyl mercaptoacetate (9.0 mL, 83.2 mmol) in 15 mL of anhydrous ether under nitrogen atmosphere was added trimethylsilyl chloride (12.0 mL, 94.6 mmol) followed by triethyl amine (13.0 mL, 93.3 mmol) slowly. White precipitates were formed upon addition of triethyl amine. The suspension was allowed to stir at room temperature overnight. The white precipitate was removed by filtration. The filtrate was concentrated on a rotavap. The residue oil was distilled at 40° C. (0.5 mm Hg) to give 10.9 g (68%) of ethyl (trimethylsilylthio)acetate as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05760048 |
| Source dataset | uspto-grants-1998_06 |
| ORD ID | ord-f50ae4673ee942fa9aacbe9f8a11eda1 |
| Source note | uspto-grants-1998_06 |