HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2238503Generated: October 26, 2026
1H-Benzotriazole-1-carboxaldehyde → {[2-Chloro-3-(trifluoromethyl)phenyl]methyl}formamide
https://huagongshe.com/reaction/2238503
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1H-Benzotriazole-1-carboxaldehyde | HCID 576740 | — |
| Reactant | 2-Chloro-3-(trifluoromethyl)benzylamine | HCID 5224207 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | {[2-Chloro-3-(trifluoromethyl)phenyl]methyl}formamide | HCID 86617531 | — |
Reaction Steps
A solution of {[2-chloro-3-(trifluoromethyl)phenyl]methyl}amine (1.05 g, 5 mmol) in anhydrous tetrahydrofuran (10 ml) was added dropwise to a solution of N-formyl benzotriazole (0.772 g, 5.25 mmol) in anhydrous tetrahydrofuran (10 ml). The reaction was stirred at 22° C. for 18 hrs then reduced in vacuo and the residue partitioned between dichloromethane (75 ml) and 2N aqueous sodium hydroxide (40 ml). The organic layer was separated and extracted with 2N aqueous sodium hydroxide (40 ml). The organic layer was passed through a hydrophobic frit and reduced in vacuo to give a white solid. The crude product was purified by automated flash silica column chromatography (Biotage SP4), eluting with a solvent gradient of 0-10% ethyl acetate in dichloromethane, to give {[2-chloro-3-(trifluoromethyl)phenyl]methyl}formamide as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07718693B2 |
|---|
| Source dataset | uspto-grants-2010_05 |
|---|
| ORD ID | ord-b6b6bc7d043f4a39a83155f795fb250c |
|---|
| Source note | uspto-grants-2010_05 |
|---|