HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1867532Generated: October 26, 2026
Diisopropylethylamine → 2-(Methylamino)-2-oxoethyl 1,1'-biphenyl-4-ylmethylcarbamate
https://huagongshe.com/reaction/1867532
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 4-Nitrophenyl chloroformate | HCID 82129 | — |
| Reactant | 2-Hydroxy-N-methylacetamide | HCID 223579 | — |
| Reactant | 4-Phenylbenzylamine | HCID 344989 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-(Methylamino)-2-oxoethyl 1,1'-biphenyl-4-ylmethylcarbamate | HCID 10402417 | — |
Reaction Steps
0.1 g (0.97 mmol) of N-methyl-2-hydroxyacetamide is admixed dropwise at ambient temperature with a solution of 0.196 g (0.97 mmol) of 4-nitrophenyl chloroformate in 3 ml of methylene chloride and 0.166 ml (0.97 mmol) of N,N-diisopropylethylamine. The mixture is stirred at ambient temperature for 45 minutes and then a solution of 0.195 g (1.067 mmol) of 4-phenylbenzylamine in 3 ml of methylene chloride and 0.166 ml (0.97 mmol) of N,N-diisopropylethylamine is added dropwise at ambient temperature. The mixture is stirred at ambient temperature for 1 hour. It is washed with saturated aqueous ammonium chloride solution, with aqueous 10% sodium carbonate solution and with saturated aqueous sodium chloride solution. The phases are separated and the organic phase is dried over sodium sulphate. The system is filtered, the filtrate is concentrated under reduced pressure and the residue is purified by chromatography on silica gel using ethyl acetate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07632850B2 |
|---|
| Source dataset | uspto-grants-2009_12 |
|---|
| ORD ID | ord-e81b64a83b3046e0870e14328cde0eb3 |
|---|
| Source note | uspto-grants-2009_12 |
|---|