HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2280675Generated: November 1, 2026
Sodium borohydride → HCID 89701791, compound
https://huagongshe.com/reaction/2280675
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 3'-Fluoro-4'-hydroxy-2',6'-dimethylbiphenyl-3-carbaldehyde | HCID 59342595 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 89701791 | HCID 89701791 | — |
Reaction Steps
3′-Fluoro-4′-hydroxy-2′,6′-dimethylbiphenyl-3-carbaldehyde 19a (700 mg, 2.87 mmol, prepared by a method disclosed in PCT patent application WO2008001931) was dissolved in 10 mL of methanol, followed by addition of sodium borohydride (130 mg, 3.44 mmol). The reaction solution was stirred for 2 hours. The resulting solution was concentrated under reduced pressure. The residue was mixed with 10 mL of water and extracted with ethyl acetate (50 mL×2). The combined organic extracts were washed with saturated sodium chloride solution (30 mL), dried with anhydrous magnesium sulphate, and filtered. The filtrate was concentrated under reduced pressure to obtain the crude title compound 3-fluoro-3′-(hydroxymethyl)-2,6-dimethylbiphenyl-4-ol 19b (700 mg) as a white solid, which was used directly in the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09139548B2 |
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| Source dataset | uspto-grants-2015_09 |
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| ORD ID | ord-ef2a9317ae334c06b27fd4b950c004e5 |
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| Source note | uspto-grants-2015_09 |
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