HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl formate → N-(4-bromo-3-methyl-benzyl)-formamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl formate | HCID 8025 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | (4-Bromo-3-methylphenyl)methanamine | HCID 21756143 | — |
| Product | N-(4-bromo-3-methyl-benzyl)-formamide | HCID 58497978 | — |
Reaction Steps
To a solution of 4-bromo-3-methyl-benzylamine (Example 10.1) (15.11 g) in ethyl formate (150 ml) was added triethylamine (1.5 ml) at ambient temperature. The reaction mixture was stirred at reflux for 16 hours. The reaction mixture was concentrated and the residue was triturated with diisopropyl ether/heptane (1:1) (100 ml) to give N-(4-bromo-3-methyl-benzyl)-formamide (14.04 g) as a white solid. 1H-NMR (400 MHz, CDCl3): 8.28 (s, 1H), 7.49 (m, 1H), 7.16 (s, 1H), 6.97 (m, 1H), 5.85 (s, 1H), 4.42 (m, 2H), 2.39 (s, 3H) ppm.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09216973B2 |
| Source dataset | uspto-grants-2015_12 |
| ORD ID | ord-655b2fb77cc04ca4953a5d16062fe106 |
| Source note | uspto-grants-2015_12 |