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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1097932Generated: October 31, 2026

Dimethyl malonate → 1-(4-Amino-2-chlorophenyl)ethan-1-one

https://huagongshe.com/reaction/1097932

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl malonateHCID 7943—
ReactantAmmonium ChlorideHCID 25517—
ReactantBenzoyl chloride, 2-chloro-4-nitro-HCID 81522—
Reactant1-(2-chloro-4-nitrophenyl)ethanoneHCID 314302—
CatalystIronHCID 23925—
SolventEthanolHCID 702—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product1-(4-Amino-2-chlorophenyl)ethan-1-oneHCID 12733837—

Reaction Steps

Iron (2.7 g), ammonium chloride (2.6 g) and water (8.1 ml) were added to a solution of 1-(2-chloro-4-nitro-phenyl)-ethanone ([CAS Reg. No. 67818-41-1], 960 mg) in ethanol (68 ml), which was made from 2-chloro-4-nitro-benzoyl chloride and malonic acid dimethyl ester according to a procedure from Dai et al.; J. Med. Chem. 2005, 48, 6066. The mixture was heated 1 h under reflux. DCM (35 ml) was added, stirred for 2 min and filtered over Celite. The residue was washed with DCM (50 ml). Water (100 ml) was added to the combined organic layers, and then extracted with DCM. The combined organic layers were dried over Na2SO4 and concentrated in vacuo to give the title compound (837 mg) as light yellow oil, which was used in the next step without further purification. MS (m/e)=170.1 [M+H+].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08143280B2
Source datasetuspto-grants-2012_03
ORD IDord-e73763f28760440db2f0682768c691ec
Source noteuspto-grants-2012_03