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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2202349Generated: October 29, 2026

Acetic Anhydride → HCID 90419163, compound

https://huagongshe.com/reaction/2202349

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantTriethylamineHCID 8471—
Reactant2-DimethylaminopyridineHCID 21885—
ReactantHCID 22975820HCID 22975820—
SolventDichloromethaneHCID 6344—
ProductHCID 90419163HCID 9041916378.8%

Reaction Conditions

Temperature20 °C

Reaction Steps

A solution of tert-butyl-4-(but-3-en-1-yl)-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), 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, purified by flash chromatography to provide the title compound 16C as colorless oil (3.4 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09365545B2
Source datasetuspto-grants-2016_06
ORD IDord-a221e4f547824be4af60525d31cc9f3d
Source noteuspto-grants-2016_06