HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trifluoroacetic acid → 2,3-Dimethyl-5-benzylthiophene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 2,3-Dimethyl-5-(alpha-hydroxybenzyl)thiophene | HCID 11637126 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 2,3-Dimethyl-5-benzylthiophene | HCID 10241963 | 94.2% |
Reaction Steps
Trifluoroacetic acid (50 mL) was added dropwise over a 60 minute period to a stirred, 0° C. suspension of 4, 5-dimethylthiophene-2-yl-(phenyl)-methanol (7.7 g, 35.3 mmol), sodium borohydride (6.67 g, 177 mmol) and ether (600 mL). After an additional 1.5 hours the reaction mixture was added to 10% aqueous sodium hydroxide (600 mL) and stirred for 30 minutes. The layers were separated and the ether phase was washed with 10% aqueous sodium hydroxide, brine and dried (magnesium sulfate). The ether phase was concentrated to provide the tide compound as a an oil (6.73 g, 94%): NMR (CDCl3); δ 7.33-7.19 (m, 5H), 6.47 (s, 1H), 4.03 (s, 2H), 2.27 (2,3H), 2.06 (s, 2H); MS (EI) (M+) 202 (45%, MI).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06444670B2 |
| Source dataset | uspto-grants-2002_09 |
| ORD ID | ord-2da0d81bf67544339fcbc303ff02ca86 |
| Source note | uspto-grants-2002_09 |