HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl chloroformate → Methyl [3,5-bis(trifluoromethyl)benzyl](2-bromo-5-fluorobenzyl)carbamate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl chloroformate | HCID 6586 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | [3,5-Bis(trifluoromethyl)benzyl](2-bromo-5-fluorobenzyl)amine | HCID 86615390 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Methyl [3,5-bis(trifluoromethyl)benzyl](2-bromo-5-fluorobenzyl)carbamate | HCID 86615391 | — |
Reaction Steps
To a solution of [3,5-bis(trifluoromethyl)benzyl](2-bromo-5-fluorobenzyl)amine from Step A (0.14 g) in methylene chloride at room temperature, excess methyl chloroformate (0.1 ml) and triethyl amine (0.1 ml) were added. The solution was stirred at room temperature for 2 h and the solvent was removed under reduced pressure. The title compound was obtained by flash column chromatography using EtOAc/hexane (1:9) as the eluant. 1H NMR (CDCl3, 500 MHz) δ 7.80 (s, 1H), 7.68 (s, 1H), 7.60 (s, 1H), 7.48 (m, 1H), 6.88 (m, 2H), 4.60 (m, 4H), 3.81 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07737295B2 |
| Source dataset | uspto-grants-2010_06 |
| ORD ID | ord-2e68953b859f4d4987dd68f6bb98408c |
| Source note | uspto-grants-2010_06 |