HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 81602Generated: October 29, 2026
Sodium borohydride → 1-(5-Bromo-2-fluorophenyl)-2,2-difluoropropane-1,3-diol
https://huagongshe.com/reaction/81602
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 55071267 | HCID 55071267 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 1-(5-Bromo-2-fluorophenyl)-2,2-difluoropropane-1,3-diol | HCID 66666261 | — |
Reaction Steps
To a solution of ethyl 3-(5-bromo-2-fluorophenyl)-2,2-difluoro-3-hydroxypropanoate (20.0 g, 61.3 mmol) in MeOH (160 mL), NaBH4 (7.0 g, 184.2 mmol) was added portion wise over a period of 30 min. at 0° C. Stirring was continued for 1 h at 0° C. and reaction was monitored by TLC. Upon complete consumption of the starting material, reaction mass was concentrated under reduced pressure and treated with saturated ammonium chloride solution. The crude reaction mass was dissolved in ethyl acetate and organic layer was washed with brine (15 mL) followed by drying over anhydrous Na2SO4. The organic layer was concentrated under reduced pressure to furnish title compound with sufficient purity. Yield=17 g (97%). TLC (50% ethyl acetate in Hexane): Rf=0.32),
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08846658B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-dc6b0facbdf14e0fb55e0b032730cbed |
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| Source note | uspto-grants-2014_09 |
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