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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 456450Generated: October 30, 2026

Acetyl chloride → 1-(3-Hydroxypiperidin-1-yl)ethan-1-one

https://huagongshe.com/reaction/456450

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetyl chlorideHCID 6367—
ReactantTriethylamineHCID 8471—
Reactant3-HydroxypiperidineHCID 23293—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
Product1-(3-Hydroxypiperidin-1-yl)ethan-1-oneHCID 2189703083.1%

Reaction Conditions

Temperature-78 °C

Reaction Steps

3-Hydroxypiperidine (3.0 g, 30.0 mmol) was dissolved in THF (40 mL) and methylene chloride (40 mL). Triethylamine (7.47 g, 74.0 mmol) was added. The mixture was cooled to −78° C. and acetyl chloride (2.35 g, 30.0 mmol) was added drop wise. The mixture was warmed to r.t. and stirred under nitrogen for 1 about an hour. The solvents were removed under reduced pressure, and the resulting oil was purified using silica chromatography (2% methanol in ethyl acetate) to afford the title compound (3.57 g, 83%) as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07186715B2
Source datasetuspto-grants-2007_03
ORD IDord-ee7f708a522c4e49b678cf3f9f315113
Source noteuspto-grants-2007_03