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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 660128Generated: November 1, 2026

Sodium Sulfide → tert-Butyl thietan-3-ylcarbamate

https://huagongshe.com/reaction/660128

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium SulfideHCID 14804—
Reactant2-[(tert-Butoxycarbonyl)amino]propane-1,3-diyl dimethanesulfonateHCID 10893393—
SolventEthanolHCID 702—
Producttert-Butyl thietan-3-ylcarbamateHCID 57415771—

Reaction Conditions

Temperature60 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08084474B2
Source datasetuspto-grants-2011_12
ORD IDord-c59cf31467f74cdaa41619d56ca6a805
Source noteuspto-grants-2011_12