HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → benzyl N-[2-(4-bromophenyl)ethyl]-N-methylcarbamate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Benzyl chloroformate | HCID 10387 | — |
| Reactant | 2-(4-Bromophenyl)-N-methylethan-1-amine | HCID 18367556 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | benzyl N-[2-(4-bromophenyl)ethyl]-N-methylcarbamate | HCID 57842600 | 65% |
Reaction Steps
Benzyl chloroformate (0.97 mL, 6.7 mmol) was added dropwise to a solution of 23B (1.1 g, 5.1 mmol)in CH2Cl2 (26 mL) and triethylamine (1 mL, 7.5 mmol). The reaction mixture washed with brine, dried over Na2SO4 and concentrated in vacuo. Purification by flash chromatography (0% to 50% EtOAc in hexanes) afforded 28C (1.15 g, 65%) as a clear oil. 1H NMR (400 MHz, CDCl3) δ ppm 2.70-2.94 (m, 5 H) 3.47 (m, 2 H) 5.08 (m, 2 H) 6.90-7.12 (m, 2 H) 7.26-7.44 (m, 7 H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07592331B2 |
| Source dataset | uspto-grants-2009_09 |
| ORD ID | ord-f4807dc20d9545a48f64f40929e2c19a |
| Source note | uspto-grants-2009_09 |