HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 66810Generated: October 26, 2026
Ethyl chloroformate → N-(1-Methyldecyl)-3-(3-Nitrophenyl)-2-butenamide
https://huagongshe.com/reaction/66810
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl chloroformate | HCID 10928 | — |
| Reactant | 2-Undecanamine | HCID 114476 | — |
| Reactant | 3-(3-Nitrophenyl)-2-butenoic acid | HCID 54402156 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | N-(1-Methyldecyl)-3-(3-Nitrophenyl)-2-butenamide | HCID 53905448 | — |
Reaction Steps
To a stirred slurry of 5.2 g. of the 3-(3-nitrophenyl)-2-butenoic acid from Preparation 12 having a melting point of 208°-210° C., in 100 ml. of dichloromethane, was added 2.8 g. of triethylamine in 10 ml. of dichloromethane. This was followed by the addition of a solution of 3.0 g. of ethyl chloroformate in 20 ml. of dichloromethane, during 20 minutes. Stirring was continued for 30 minutes, and then a solution of 1-methyldecylamine in 20 ml. of dichloromethane was added dropwise during 25 minutes. Stirring was continued overnight, and the the reaction mixture was washed successively with 1 N potassium carbonate, water and saturated sodium chloride. The resulting solution was dried using sodium sulfate, and then it was evaporated in vacuo leaving an oil which solidified on trituration under petroleum ether. This afforded 4.9 g. of the title compound, m.p. 72.5°-74° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04343813 |
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| Source dataset | uspto-grants-1982_08 |
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| ORD ID | ord-921caf7094484586aeaa6606fc5056d7 |
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| Source note | uspto-grants-1982_08 |
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