HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → HCID 53822308, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Methanol | HCID 887 | — |
| Reactant | 3-Phenoxybenzaldehyde | HCID 38284 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Product | HCID 53822308 | HCID 53822308 | 100% |
Reaction Steps
Sodium borohydride (961 mg, 25.3 mmol) was added in one portion to a solution of 3-phenoxybenzaldehyde (10.0 g, 50.5 mmol) in methanol (150 mL) at RT under argon. Once the bubbling ceased, the reaction was stirred at RT for 5 min, then adjusted to pH 6 with glacial acetic acid (about 1 mL). The reaction was concentrated in vacuo to give a residue, which was partitioned between EtOAc (200 mL) and saturated NaHCO3 (50 mL). The organic layer was washed with water and brine (50 mL each), then dried over MgSO4. Evaporation gave title compound (10.1 g, 100%) as a tan oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05470845 |
| Source dataset | uspto-grants-1995_11 |
| ORD ID | ord-aa0fe1a4e0a74124b98945026df568be |
| Source note | uspto-grants-1995_11 |