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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 404740Generated: October 30, 2026

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

https://huagongshe.com/reaction/404740

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl 4-bromopiperidine-1-carboxylateHCID 15541517—
ReactantPotassium ethanethioateHCID 23670855—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Producttert-Butyl 4-(acetylthio)piperidine-1-carboxylateHCID 2249477382.9%

Reaction Conditions

Temperature100 °C

Reaction Steps

2.2 g (19.3 mmol) Potassium thioacetate and 2.65 g (10 mmol) 4-Bromo-piperidine-1-carboxylic acid tert-butyl ester were dissolved in 50 ml of DMF and stirred at 100° C. for 4 h. The mixture was taken up in ethyl acetate and washed with brine. The organic phases were dried over Sodium sulfate and evaporated. Purification over silica gel (10% to 20% ethyl acetate in heptane) gave 2.15 g of the expected compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08748614B2
Source datasetuspto-grants-2014_06
ORD IDord-05a02250546e4fd5a5cb2153cf9297d0
Source noteuspto-grants-2014_06