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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1092859Generated: November 3, 2026

Water → tert-Butyl 4-(acetylthio)piperidine-1-carboxylate

https://huagongshe.com/reaction/1092859

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactanttert-Butyl methyl etherHCID 15413—
Reactant1-(tert-Butoxycarbonyl)-4-(methanesulfonyloxy)piperidineHCID 4184869—
ReactantPotassium ethanethioateHCID 23670855—
SolventDimethylformamideHCID 6228—
Producttert-Butyl 4-(acetylthio)piperidine-1-carboxylateHCID 22494773—

Reaction Conditions

Temperature65 °C

Reaction Steps

Crude 4-methanesulfonyloxy-piperidine-1-carboxylic acid tert-butyl ester was dissolved in 200 ml DMF, and potassium thioacetate (18.5 g, 162 mmol) was added. The mixture was stirred overnight under a nitrogen atmosphere at about 65° C. The reaction mixture solidified overnight, and after it was cooled to room temperature, 250 ml water and 250 ml TBME was added, and the mixture was stirred for 10 minutes. The layers were separated, and the aqueous layer was extracted with 200 ml TBME. The combined organic layers were washed with water (2×250 ml) and saturated aqueous NaCl solution (150 ml), dried over sodium sulfate, filtered, and evaporated to dryness (30.3 g, 94%) to give a dark-brown oil identified as the product by 1H-NMR, which was used without purification in the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08129546B2
Source datasetuspto-grants-2012_03
ORD IDord-8b4354b794144167b4fa9b51b8224315
Source noteuspto-grants-2012_03