HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → Acetamide, N-[(2-bromophenyl)methyl]-2,2,2-trifluoro-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethyl trifluoroacetate | HCID 9794 | — |
| Reactant | 2-Bromobenzylamine | HCID 334072 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Acetamide, N-[(2-bromophenyl)methyl]-2,2,2-trifluoro- | HCID 57470274 | 103.4% |
Reaction Steps
To a solution of 2-bromobenzylamine (1.3 mL, 10.8 mmol) in methanol (5 mL) was added ethyl trifluoroacetate (1.54 mL, 21.6 mmol) and triethylamine (1.4 mL, 10.8 mmol) under a nitrogen atmosphere. The reaction was stirred at room temperature for 1 h. The reaction mixture was then concentrated under vacuum to yield N-(2-bromo-benzyl)-2,2,2-trifluoro-acetamide (3.15 g, quant.). HPLC ret. time 2.86 min, 10-99% CH3CN, 5 min run; ESI-MS 283.9 m/z (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08829204B2 |
| Source dataset | uspto-grants-2014_09 |
| ORD ID | ord-a58ea110164e4951bae5340068fc0d41 |
| Source note | uspto-grants-2014_09 |