HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → (4-(3-(Trifluoromethyl)phenoxy)phenyl)methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 4-(3-(Trifluoromethyl)phenoxy)benzaldehyde | HCID 12148788 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | (4-(3-(Trifluoromethyl)phenoxy)phenyl)methanol | HCID 66825531 | 121.4% |
Reaction Steps
A solution of 4-{[3-(Trifluoromethyl)phenyl]oxy}benzaldehyde (4.1 g, 9.55 mmol) in methanol (50 mL) at 0° C. was added sodium borohydride (1.0 g, 26.4 mmol) in portions. The reaction mixture was allowed to warm to rt and stirred for 1 h, then quenched with acetone, concentrated. Purification via ISCO system afforded the title product (3.11 g) as a colorless liquid. LC-MS (ESI): m/z 251 [M-OH]+; 3.23 min (ret time).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08859573B2 |
| Source dataset | uspto-grants-2014_10 |
| ORD ID | ord-7412d11c45af43de87020817d2bfe525 |
| Source note | uspto-grants-2014_10 |