HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 547287Generated: October 31, 2026
Sodium methanethiolate → HCID 86064723, compound
https://huagongshe.com/reaction/547287
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium methanethiolate | HCID 4378561 | — |
| Reactant | tert-butyl N-{2-[2-(methanesulfonyloxy)ethoxy]ethyl}carbamate | HCID 12106196 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 86064723 | HCID 86064723 | 96.6% |
Reaction Steps
A suspension of 2-{2-[(tert-butoxycarbonyl)amino]ethoxy}ethyl methanesulfonate (28 g, 99 mmol) and sodium thiomethoxide (8.3 g, 119 mmol) in N,N-dimethylformamide (DMF, 200 mL) was heated to 80° C. and maintained at that temperature until analysis by thin layer chromatography (TLC) indicated that the starting material had been consumed. The reaction mixture was allowed to cool to ambient temperature and was then quenched with water (200 mL). The reaction mixture was extracted with diethyl ether (2×200 mL). The combined extracts were washed sequentially with saturated aqueous sodium bicarbonate (100 mL) and brine (100 mL), dried over anhydrous sodium sulfate, filtered, and then concentrated under reduced pressure to provide 22.5 g of tert-butyl 2-[2-(methylthio)ethoxy]ethylcarbamate as a light yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07939526B2 |
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| Source dataset | uspto-grants-2011_05 |
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| ORD ID | ord-2956082bb87a4100ad483657a6379cc9 |
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| Source note | uspto-grants-2011_05 |
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