HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 333831Generated: October 31, 2026
Dimethyl malonate → 1-(4-Amino-2-chlorophenyl)ethan-1-one
https://huagongshe.com/reaction/333831
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl malonate | HCID 7943 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Benzoyl chloride, 2-chloro-4-nitro- | HCID 81522 | — |
| Reactant | 1-(2-chloro-4-nitrophenyl)ethanone | HCID 314302 | — |
| Catalyst | Iron | HCID 23925 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-(4-Amino-2-chlorophenyl)ethan-1-one | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08883786B2 |
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| Source dataset | uspto-grants-2014_11 |
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| ORD ID | ord-4455f5f37b494753ae403c4a4a44558f |
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| Source note | uspto-grants-2014_11 |
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