HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2060941Generated: October 31, 2026
Sodium Sulfide → tert-Butyl thietan-3-ylcarbamate
https://huagongshe.com/reaction/2060941
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Sulfide | HCID 14804 | — |
| Reactant | 2-[(tert-Butoxycarbonyl)amino]propane-1,3-diyl dimethanesulfonate | HCID 10893393 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | tert-Butyl thietan-3-ylcarbamate | HCID 57415771 | — |
Reaction Steps
A solution of N-(tert-butyloxycarbonyl)-2-amino-1,3-propanediol dimesylate [prepared according to E. Benoist et al., Synthesis 1998, (8), 1113-1118] (25 g, 72.0 mmol) in ethanol (375 ml) is treated with sodium sulfide (Na2S.xH2O 32-38%, 16.82 g, ˜75.4 mmol) and the mixture is stirred at a temperature of 50° C. (bath 60° C.) for 45 minutes. The cooled reaction mixture is concentrated under reduced pressure and the solid residue poured into water, extracted with Et2O, the combined organic layers washed with brine, dried (Na2SO4), filtered, and concentrated. The crude solid product (12.6 g, 92%) is used in the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08278464B2 |
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| Source dataset | uspto-grants-2012_10 |
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| ORD ID | ord-518b583c7c854ae6b2ca7b7d677f6179 |
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| Source note | uspto-grants-2012_10 |
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