HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1785134Generated: October 31, 2026
Triethylamine → 4-Nitrophenyl methyl(prop-2-yn-1-yl)carbamate
https://huagongshe.com/reaction/1785134
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-Nitrophenyl chloroformate | HCID 82129 | — |
| Reactant | N-methylpropyn-2-ylamine | HCID 96160 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-Nitrophenyl methyl(prop-2-yn-1-yl)carbamate | HCID 85912913 | 89% |
Reaction Steps
N-Methylpropargylamine (600 mg, 8.70 mmol) and triethylamine (878 mg, 8.68 mmol) in dichloromethane (10 ml) were added dropwise, with ice cooling, to a stirred solution of 4-nitrophenyl chloroformate (1.75 g, 8.68 mmol) in dichloromethane (10 ml). The reaction was stirred at ice temperature for 3 hr. then the resulting solution purified by column chromatography on silica using 25% ethyl acetate in iso-hexane as eluent. Thus was obtained 4-nitrophenyl methyl(prop-2-yn-1-yl)carbamate (1.80 g, 89%) as a colourless oil. Dimethylamine (3.0 ml of a 2.0M solution in THF, 6.0 mmol) and 4-nitrophenyl methyl(prop-2-yn-1-yl)carbamate (600 mg, 2.56 mmol), in dichloromethane (7 ml) were stirred at room temperature for 6 days then the reaction solution purified by chromatography on silica using ethyl acetate as eluent to give N,N,N′-trimethyl-N′-prop-2-yn-1-ylurea (164 mg, 46%) as a colourless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07504408B2 |
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| Source dataset | uspto-grants-2009_03 |
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| ORD ID | ord-57cfa8b9b39645b091a0818a65886850 |
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| Source note | uspto-grants-2009_03 |
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