HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2251708Generated: October 25, 2026
Water → Dimethyl 2-(4-chlorobenzoylamino)malonate
https://huagongshe.com/reaction/2251708
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 4-Chlorobenzoyl chloride | HCID 8501 | — |
| Reactant | Dimethyl 2-aminomalonate hydrochloride | HCID 2734846 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Dimethyl 2-(4-chlorobenzoylamino)malonate | HCID 68614697 | 79% |
Reaction Steps
Part A: To a stirred solution of dimethyl aminomalonate hydrochloride (25 gram, 0.136 mol) in dichloromethane (200 mL) triethylamine (41.4 mL, 2.2 molar equivalent) is added at 0° C. 4-Chlorobenzoyl chloride (23.8 gram, 0.136 mol) is slowly added and the resulting solution is allowed to stand at room temperature overnight. Water is added and the organic layer is separated. The water layer is extracted twice with dichloromethane. The collected organic layers are washed with water, dried over MgSO4, filtered and concentrated in vacuo. The residue is recrystallised from methanol (400 mL) to give dimethyl 2-(4-chlorobenzoylamino)malonate (30.5 gram, 79% yield). Melting point: 146-148° C. 1H-NMR (200 MHz, CDCl3): δ 3.86 (s, 6H), 5.38 (d, J=6 Hz, 1H), 7.15 (br d, J˜6 Hz, 1H), 7.43 (d, J=8 Hz, 2H), 7.79 (d, J=8 Hz, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07319110B2 |
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| Source dataset | uspto-grants-2008_01 |
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| ORD ID | ord-32fa02d866454be2ad382e22270dd4b4 |
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| Source note | uspto-grants-2008_01 |
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