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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1770640Generated: November 2, 2026

Sodium sulfide monohydrate → HCID 71271685, compound

https://huagongshe.com/reaction/1770640

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium sulfide monohydrateHCID 19906495—
ReactantHCID 86725181HCID 86725181—
SolventMethanolHCID 887—
ProductHCID 71271685HCID 7127168521.5%

Reaction Conditions

Temperature40 °C

Reaction Steps

To a solution of crude methanesulfonic acid 1-(tert-butoxycarbonylamino-methyl)-3-methanesulfonyloxy-propyl ester (1.24 g) in methanol (25 ml) was added sodium sulfide monohydrate (0.84 g). The reaction mixture was stirred at 40° C. for 3 hours. The methanol was partially removed by distillation. Water was added and the mixture was extracted three times with ethyl acetate. The organic phases were combined, dried over anhydrous sodium sulfate and concentrated. The residue was purified over silica gel (ethyl acetate/heptanes, from 1:4 to 1:1) to give thietan-2-ylmethyl-carbamic acid tert-butyl ester (0.15 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09247740B2
Source datasetuspto-grants-2016_02
ORD IDord-0b09d8596b5741b6a733b6898fef28e4
Source noteuspto-grants-2016_02