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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1267697Generated: October 29, 2026

4-Chlorobutyryl chloride → HCID 12051895, compound

https://huagongshe.com/reaction/1267697

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Chlorobutyryl chlorideHCID 78370—
ReactantAluminum(III) ChlorideHCID 6451240—
ReactantN-Methoxy-N-methyl-2-phenyl-isobutyramideHCID 59788661—
SolventDichloromethaneHCID 6344—
ProductHCID 12051895HCID 1205189563%

Reaction Steps

Slurry AlCl3 (10.15 g, 76.1 mmol) and methylene chloride (45 mL) under a nitrogen atmosphere at room temperature. Add 4-chlorobutyryl chloride (4.27 mL, 38.1 mmol), stir for 20 minutes and add, by dropwise addition over 10 minutes, a solution of 2-methyl-2-phenyl-propionic acid, N-methoxy-N-methylamide (6.58 g, 31.7 mmol) in methylene chloride (15 mL). Stir at room temperature for 45 minutes, then heat at 30-35° C. for 7 hours. Pour into ice water (150 mL) and separate the layers. Wash the aqueous layer with water (3×75 mL), combine the aqueous layers and extract with methylene chloride (2×75 mL). Combine the organic layers and dry (Na2SO4). Filter, evaporate the filtrate in vacuo and purify by silica gel chromatography (3:1 hexane/ethyl acetate) give the title compound (6.19 g, 63%) as a light yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06552200B2
Source datasetuspto-grants-2003_04
ORD IDord-4196d4947b194d0a85983dc96e29927b
Source noteuspto-grants-2003_04