Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2202401Generated: October 31, 2026

Acetic Anhydride → HCID 90419021, compound

https://huagongshe.com/reaction/2202401

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantTriethylamineHCID 8471—
Reactant2-DimethylaminopyridineHCID 21885—
ReactantTert-butyl 4-allyl-4-hydroxypiperidine-1-carboxylateHCID 21955339—
SolventDichloromethaneHCID 6344—
ProductHCID 90419021HCID 9041902182.7%

Reaction Conditions

Temperature20 °C

Reaction Steps

A solution of tert-butyl 4-allyl-4-hydroxypiperidine-1-carboxylate (3.7 g, 14.51 mmol) in dichloromethane (20 mL) was treated with dimethylaminopyridine (1.8 g, 14.51 mmol), acetic anhydride (4.1 mL, 43.53 mmol) and triethylamine (6.1 mL, 43.53 mmol), and was stirred overnight at 20° C. The solvent was removed under reduced pressure and the residue was partitioned between water and ethyl acetate. The aqueous layer was extracted twice with ethyl acetate. Combined organic extracts were washed with water, dried (Na2SO4) and filtered. The filtrate was concentrated under reduced pressure, and purified by a standard method to provide the title compound 44B (3.4 g). LC-MS: m/z 284.4 (M+H)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09365545B2
Source datasetuspto-grants-2016_06
ORD IDord-4dae177b7d3f49e481c5cf539b3b9ec9
Source noteuspto-grants-2016_06