HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 981262Generated: October 25, 2026
N-Methyl-N-nitrosourea → Ethyl 4-(1-diphenylmethoxycarbonyl-2-methylvinyl)-2,3,5-trifluorobenzoate
https://huagongshe.com/reaction/981262
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N-Methyl-N-nitrosourea | HCID 12699 | — |
| Reactant | Ethyl 4-(1-diphenylmethoxycarbonylvinyl)-2,3,5-trifluorobenzoate | HCID 10094769 | — |
| Reactant | Diazomethane diethylether | HCID 21186548 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | Ethyl 4-(1-diphenylmethoxycarbonyl-2-methylvinyl)-2,3,5-trifluorobenzoate | HCID 53699771 | 91.2% |
Reaction Steps
In 30 ml of diethyl ether was dissolved 3.08 g of ethyl 4-(1-diphenylmethoxycarbonylvinyl)-2,3,5-trifluorobenzoate. To the resulting solution was added, with ice-cooling, a diazomethane-diethyl ether solution prepared from 2.00 g of N-methyl-N-nitrosourea. The resulting mixture was stirred at room temperature for 12 hours. The reaction mixture was concentrated under reduced pressure. The residue obtained was dissolved in 30 ml of toluene. The resulting solution was stirred at 60° C. for 1 hour. The reaction mixture was concentrated under reduced pressure. The residue obtained was purified by a column chromatography (eluant: toluene) to obtain 2.90 g (yield: 91.2%) of ethyl 4-(1-diphenylmethoxycarbonyl-2-methylvinyl)-2,3,5-trifluorobenzoate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04990508 |
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| Source dataset | uspto-grants-1991_02 |
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| ORD ID | ord-7bcda04aa6404bc5b49aa9278aab87c3 |
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| Source note | uspto-grants-1991_02 |
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