HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1430410Generated: October 25, 2026
Dimethylacetamide → 8-Benzyloxy-1,3,3-trimethyl-1,5-dihydrobenzo[b][1,4]diazepine-2,4-dione
https://huagongshe.com/reaction/1430410
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylacetamide | HCID 31374 | — |
| Reactant | Dimethylmalonyl Dichloride | HCID 4523180 | — |
| Reactant | 5-benzyloxy-N1-methylbenzene-1,2-diamine hydrochloride | HCID 67953976 | — |
| Solvent | Water | HCID 962 | — |
| Product | 8-Benzyloxy-1,3,3-trimethyl-1,5-dihydrobenzo[b][1,4]diazepine-2,4-dione | HCID 67954154 | 83% |
Reaction Steps
Under ice cooling, dimethylmalonic acid dichloride (9.9 mL, 74.9 mmol) was added dropwise to a N,N-dimethyl acetamide (90 mL) solution of 5-benzyloxy-N1-methylbenzene-1,2-diamine hydrochloride (18.0 g, 68.0 mmol). The mixture was stirred at the same temperature for 2.5 hours, and water (90 mL) was added thereto. The reaction solution was stirred at 10° C. or less for 30 minutes, and precipitated crystals were collected by filtration. The resulting crystals were washed with water, then added to methanol (180 mL), and heated under reflux. The mixture was cooled and stirred at 10° C. or less for 30 minutes, and precipitated crystals were collected by filtration. The resulting crystals were washed with methanol (36 mL), and dried at 60° C., thereby obtaining 18.3 g of a white, powdery target compound (yield: 83%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08940889B2 |
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| Source dataset | uspto-grants-2015_01 |
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| ORD ID | ord-43f382f4fe15413ea4db9d3e3ae7daa2 |
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| Source note | uspto-grants-2015_01 |
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