HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1470662Generated: November 3, 2026
Sodium borohydride → 2,3,5,6-Tetrafluoro-4'-hydroxymethyl-biphenyl-4-carboxylic acid methyl ester
https://huagongshe.com/reaction/1470662
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 2,3,5,6-Tetrafluoro-4'-formyl-biphenyl-4-carboxylic acid methyl ester | HCID 58073939 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 2,3,5,6-Tetrafluoro-4'-hydroxymethyl-biphenyl-4-carboxylic acid methyl ester | HCID 58073924 | 86.9% |
Reaction Steps
2,3,5,6-Tetrafluoro-4′-formyl-biphenyl-4-carboxylic acid methyl ester (1.26 g, 4.03 mmol) was dissolved in methanol (30 mL) and cooled to −10° C. Sodium borohydride (0.76 g, 20.19 mmol) was added portion wise and reaction mixture stirred by maintaining the same temperature. The progress of the reaction was monitored by TLC. After completion, the reaction mixture was concentrated to dryness. The obtained residue was redissolved in ethyl acetate (50 mL) and washed with water (20 mL×2) followed by brine, dried over anhydrous sodium sulphate and concentrated to get colorless solid (1.1 g, 86.75%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09006454B2 |
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| Source dataset | uspto-grants-2015_04 |
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| ORD ID | ord-ca523cb9a0a64791bc519b4763ff9765 |
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| Source note | uspto-grants-2015_04 |
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