Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl formate | HCID 8025 | — |
| Reactant | (3-Bromo-4-fluorophenyl)methanamine | HCID 2724902 | — |
| Product | HCID 58092086 | HCID 58092086 | 69.8% |
Reaction Steps
Formic acid ethyl ester (1.48 g) was added dropwise to 1-(3-bromo-4-fluorophenyl)methanamine (3.40 g) that was being stirred under ice cooling (0° C.). The reaction mixture was stirred as it was for 2 hours, then was returned to room temperature, and stirred for another 2 hours. The reaction mixture was directly subjected to purification by silica gel chromatography, to obtain N-(3-bromo-4-fluorobenzyl)formamide (2.7 g) at a yield of 69%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08304371B2 |
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| Source dataset | uspto-grants-2012_11 |
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| ORD ID | ord-d267f9c41a924b7fa44477e836251ddd |
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| Source note | uspto-grants-2012_11 |
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