HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2171343Generated: November 1, 2026
Sodium borohydride → (4-((6-Chloropyridin-3-yl)oxy)-3-fluorophenyl)methanol
https://huagongshe.com/reaction/2171343
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 4-((6-Chloropyridin-3-yl)oxy)-3-fluorobenzaldehyde | HCID 86724192 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | (4-((6-Chloropyridin-3-yl)oxy)-3-fluorophenyl)methanol | HCID 86676396 | — |
Reaction Steps
To a solution of 4-((6-chloropyridin-3-yl)oxy)-3-fluorobenzaldehyde (2.80 g, 11.1 mmol) in methanol (25 mL) was added portionwise solid NaBH4 (0.842 g, 22.3 mmol) at room temperature. The reaction mixture was stirred at 25° C. for 2 h, concentrated to remove solvent, dissolved in water (50 mL) and extracted with ethyl acetate (50 mL×2). Combined organic parts were washed with brine, dried over anhydrous Na2SO4, filtered and concentrated. The crude was used into next step without purification (2.8 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09051325B2 |
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| Source dataset | uspto-grants-2015_06 |
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| ORD ID | ord-b27902b7a0314f36aa75815c99f5066a |
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| Source note | uspto-grants-2015_06 |
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