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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2202079Generated: October 26, 2026

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

https://huagongshe.com/reaction/2202079

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 numberUS09365519B2
Source datasetuspto-grants-2016_06
ORD IDord-a3884957cdff4ef0b32ae3adbf2b9e83
Source noteuspto-grants-2016_06