HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → N-phenoxycarbonyl-(R)-2-(2, 3-methylenedioxyphenyl) heptylamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Phenyl chloroformate | HCID 15891 | — |
| Reactant | (R)-2-(2, 3-methylenedioxyphenyl) heptylamine | HCID 10331642 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | N-phenoxycarbonyl-(R)-2-(2, 3-methylenedioxyphenyl) heptylamine | HCID 54262691 | 98.9% |
Reaction Steps
To a mixture of 2.35 g of (R)-2-(2, 3-methylenedioxyphenyl) heptylamine, 1.20 g of triethylamine and 20 ml of ethyl acetate was dropwise added 1.72 g of phenyl chloroformate with ice cooling and stirring, and the resultant mixture was stirred at room temperature for 2 hours. The reaction mixture was washed with water and saturated saline in this order, dried over anhydrous sodium sulfate and the solvent evaporated to give 3.51 g of N-phenoxycarbonyl-(R)-2-(2, 3-methylenedioxyphenyl) heptylamine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05442060 |
| Source dataset | uspto-grants-1995_08 |
| ORD ID | ord-01d1182842f141eaa9bc45a31711cee7 |
| Source note | uspto-grants-1995_08 |