HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → HCID 57739004, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 22227324 | HCID 22227324 | — |
| Solvent | Npc112006 | HCID 21965192 | — |
| Product | HCID 57739004 | HCID 57739004 | 70% |
Reaction Steps
To a solution of 4-(trifluorovinyloxy)benzaldehyde (about 35 mmol) in benzene/ethanol (75/75 mL) at room temperature was added sodium borohydride (1.8 g, 1.3 eq). The resulting mixture was stirred at room temperature for 3 h. Under reduced pressure, all the solvent was evaporated. The residue was extracted by CH2Cl2 for 1 h and dried over sodium sulfate. The product was purified by chromatography using CH2Cl2 as the eluent to afford 4-(trifluorovinyloxy)benzyl alcohol as colorless oil (5.0 g, yield 68%). 1H NMR (CDCl3): δ 7.36 (d, J=8.8 Hz, 2H), 7.09 (d, J=8.8 Hz, 2H), 4.67 (s, 2H), 2.03 (s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07019453B2 |
| Source dataset | uspto-grants-2006_03 |
| ORD ID | ord-11da16b25528478d88b02af9d5a4bac5 |
| Source note | uspto-grants-2006_03 |