HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 633611Generated: October 27, 2026
Water → Diethyl 2-(4-methoxy-3,5-dimethylbenzoylamino)malonate
https://huagongshe.com/reaction/633611
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Propanedioic acid, 2-amino-, 1,3-diethyl ester, hydrochloride (1:1) | HCID 3084143 | — |
| Reactant | 3,5-Dimethyl-4-methoxybenzoyl chloride | HCID 21435383 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Diethyl 2-(4-methoxy-3,5-dimethylbenzoylamino)malonate | HCID 67294070 | — |
Reaction Steps
58.4 g of diethyl aminomalonate hydrochloride were suspended in 300 ml of dichloromethane, and 115 ml of triethylamine were added with ice cooling. At 0° C., 54.8 g of 4-methoxy-3,5-dimethylbenzoyl chloride in 250 ml of dichloromethane were then added dropwise. After 2 hours at 0° C., 100 ml of water were added dropwise, and the aqueous phase was separated off and extracted with 200 ml of dichloromethane. The combined organic phases were extracted first with 2M aqueous hydrochloric acid and then with water, dried over sodium sulfate, filtered and concentrated. The residue was triturated with methyl tert-butyl ether, filtered off with suction and dried under reduced pressure. This gave 89.3 g (96%) of the title compound which was reacted further without any further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09321787B2 |
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| Source dataset | uspto-grants-2016_04 |
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| ORD ID | ord-14d820cb479b4378a9649a4dc203eda0 |
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| Source note | uspto-grants-2016_04 |
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