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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 624278Generated: November 2, 2026

Acetyl chloride → Tert-butyl 4-(4-acetamidophenylthio)piperidine-1-carboxylate

https://huagongshe.com/reaction/624278

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetyl chlorideHCID 6367—
ReactantTriethylamineHCID 8471—
ReactantTert-butyl 4-(4-aminophenylthio)piperidine-1-carboxylateHCID 18538812—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductTert-butyl 4-(4-acetamidophenylthio)piperidine-1-carboxylateHCID 68752092—

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a 10 mL round-bottomed flask was added tert-butyl 4-(4-aminophenylthio)piperidine-1-carboxylate (100 mg, 0.324 mmol) and triethylamine (249 μl, 1.783 mmol) in dichloromethane (3242 μl). The mixture was cooled to −78° C. and acetyl chloride (115 μl, 1.621 mmol) was added. The solution was warmed to room temperature, stirred for 1 h and then diluted with water and additional dichloromethane. The aqueous phase was extracted twice with dichloromethane and the combined organics were dried with sodium sulfate, filtered and concentrated to give the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09302989B2
Source datasetuspto-grants-2016_04
ORD IDord-b2f3763f6c3244079a729d30c90f60d0
Source noteuspto-grants-2016_04