HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1499579Generated: November 1, 2026
3,5-Difluorobenzaldehyde → 3,5-Difluorobenzyl alcohol
https://huagongshe.com/reaction/1499579
Participants
| Role | Name | HCID | Charge |
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| Reactant | 3,5-Difluorobenzaldehyde | HCID 588160 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 3,5-Difluorobenzyl alcohol | HCID 522721 | — |
Reaction Steps
To a solution of 3,5-difluorobenzaldehyde (2.00 g, 14.1 mmol) in MeOH (20 mL) at 0-5° C. was added NaBH4 (1.06 g, 28.1 mmol) portionwise. The mixture was stirred at 0-5° C. for 1 h, quenched with brine, and then extracted with EtOAc (2×). The combined organic phases were washed with water and brine, then dried over Na2SO4 and concentrated under reduced pressure to give sub-title compound as a colorless oil. %). 1H NMR (300 MHz, CDCl3) δ 6.88 (m, 2H), 6.70 (m, 1H), 4.69 (s, 2H), 1.88 (br s, 1H) ppm.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09200004B2 |
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| Source dataset | uspto-grants-2015_12 |
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| ORD ID | ord-1e8cd699dd444c3db7e420ab3ce7a7a5 |
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| Source note | uspto-grants-2015_12 |
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