HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → E-{5-Fluoro-2-[2-(4-methoxyphenyl)vinyl]phenyl}methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | E-5-Fluoro-2-[2-(4-methoxyphenyl)vinyl]benzaldehyde | HCID 57831341 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | E-{5-Fluoro-2-[2-(4-methoxyphenyl)vinyl]phenyl}methanol | HCID 57831377 | 86.6% |
Reaction Steps
1.73 g (45.60 mmol) of sodium borohydride are added in portions to a solution of 7.79 g (30.40 mmol) of E-5-fluoro-2-[2-(4-methoxyphenyl)vinyl]benzaldehyde from Example 29A in 500 ml of methanol at 0° C., and the mixture is stirred at room temperature for 2 hours. After reaction is complete, the mixture is concentrated to dryness and then taken up in water and dichloromethane. The aqueous phase is then extracted twice more with dichloromethane. The combined organic phases are dried over sodium sulfate, filtered and concentrated to dryness. The resulting residue is purified by flash chromatography on silica gel (mobile phase: cyclohexane/ethyl acetate 4:1→1:1). 6.8 g (85% yield) of a colorless solid are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07998988B2 |
| Source dataset | uspto-grants-2011_08 |
| ORD ID | ord-2972fe19eb314e09a9e1aadfd3b50740 |
| Source note | uspto-grants-2011_08 |