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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 261499Generated: November 1, 2026

Acetyl chloride → 2,3-Dihydro-1'-acetylspiro[benzofuran-2,4'-piperidine]

https://huagongshe.com/reaction/261499

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetyl chlorideHCID 6367—
ReactantSodium BicarbonateHCID 516892—
Reactant3H-Spiro(1-benzofuran-2,4'-piperidine)HCID 12733230—
SolventChloroformHCID 6212—
Product2,3-Dihydro-1'-acetylspiro[benzofuran-2,4'-piperidine]HCID 12733234—

Reaction Steps

3 ml of acetyl chloride in 10 ml of chloroform are added dropwise to a stirred suspension of 6.0 g of 2,3-dihydrospiro[benzofuran-2,4'-piperidine], Example 7, and 14.0 g of sodium bicarbonate in 75 ml of chloroform. After total addition, the reaction mixture is successively stirred at ambient temperature for 16 hours, filtered, washed sequentially with water, dilute hydrochloric acid and a saturated sodium chloride solution, dried and the solvent is removed under reduced pressure, leaving a residue which solidifies upon standing. The solid is recrystallized twice from hexane to give the product, 2,3-dihydro-1'-acetylspiro[benzofuran-2,4'-piperidine], mp 94°-97° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04166119
Source datasetuspto-grants-1979_08
ORD IDord-bf4304d8b0344aa49324e93f937d7992
Source noteuspto-grants-1979_08