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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2211126Generated: November 2, 2026

4-Chlorobutyryl chloride → HCID 15292528, compound

https://huagongshe.com/reaction/2211126

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Chlorobutyryl chlorideHCID 78370—
ReactantAluminum(III) ChlorideHCID 6451240—
Reactant3-acetyl-2,3,4,5-tetrahydro-1H-3-benzazepineHCID 19375487—
SolventDichloromethaneHCID 6344—
ProductHCID 15292528HCID 1529252891.8%

Reaction Conditions

Temperature20 °C

Reaction Steps

In 30 ml of dichloromethane, was dissolved 3.79 g of 3-acetyl-2,3,4,5-tetrahydro-1H-3-benzazepine. To the solution were added 3.38 g of 4-chlorobutyryl chloride and 4.00 g of aluminum chloride. The mixture was stirred for 2 hours at room temperature (about 20° C.). The reaction mixture was poured into 50 ml of ice-water. The organic layer was separated, which was washed successively with 50 ml of 0.5N aqueous solution of sodium hydroxide and 50 ml of pure water, then dried over anhydrous sodium sulfate. The solvent was distilled off to leave 5.40 g of an oily residue. The residue was purified by means of a silica gel column chromatography (developing solvent, ethyl acetate-dichloromethane 1:1 (V/V)) to afford 2.92 g of the title compound as colorless crystals, m.p.103°-106° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05462934
Source datasetuspto-grants-1995_10
ORD IDord-ac4ffbf5f00a44ebbdb8ca4507ca6e45
Source noteuspto-grants-1995_10