HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Phenyl-5-(trifluoromethyl)thiophene-2-carboxylic acid → (4-Phenyl-5-(trifluoromethyl)thiophen-2-yl)methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Phenyl-5-(trifluoromethyl)thiophene-2-carboxylic acid | HCID 2783372 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (4-Phenyl-5-(trifluoromethyl)thiophen-2-yl)methanol | HCID 2781490 | 98.1% |
Reaction Steps
A solution of 2.10 g (7.7 mmol) of 4-phenyl-5-trifluoromethyl-thiophene-2-carboxylic acid (Step C) in 20 mL of THF was treated with 5.0 mL of 2.0 M borane dimethylsulfide complex in THF. The resulting solution was heated at reflux for 3 h, cooled to rt, quenched with 10 mL of MeOH and concentrated. Chromatography on a Biotage 40M cartridge using 9:1 v/v hexanes/ethyl acetate as the eluant afforded 1.95 g (98%) of the title compound: 1H NMR (500 MHz) δ 2.05 (app s, 1H), 4.87 (s, 2H), 6.99 (s, 1H), 7.41 (app s, 5H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07220734B2 |
| Source dataset | uspto-grants-2007_05 |
| ORD ID | ord-2d69b91549384404964656e42ce69602 |
| Source note | uspto-grants-2007_05 |