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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 880337Generated: October 26, 2026

Acetic Anhydride → tert-Butyl (1-acetylpiperidin-4-yl)carbamate

https://huagongshe.com/reaction/880337

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantTriethylamineHCID 8471—
Reactant4-(N-Boc-amino)piperidineHCID 723833—
SolventDichloromethaneHCID 6344—
Producttert-Butyl (1-acetylpiperidin-4-yl)carbamateHCID 22741830—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of tert-butyl piperidin-4-ylcarbamate (200 g, 1 mol) and Et3N (150 g, 1.5 mol) in DCM (3000 mL) was added Ac2O (102 g, 1 mol) dropwise over 1 h, while maintained the temperature at 0° C. After addition, the mixture was stirred 0° C. for another 2 h, at which time TLC showed the reaction was completed. The solution was quenched by addition of water (1 L). The organic phase was collected and washed with saturated aqueous NaHCO3 (1 L), dried (Na2SO4) and concentrated to give crude product. Four batches were run in parallel and produced a combined crude product weight of 670 g. This crude was used directly in the step. LCMS (m/z): 243.1 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08993555B2
Source datasetuspto-grants-2015_03
ORD IDord-a9936dac0d6e4eb3b3d2080ed920ec4d
Source noteuspto-grants-2015_03