HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1771807Generated: November 2, 2026
Sodium borohydride → HCID 89443811, compound
https://huagongshe.com/reaction/1771807
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 3′,4-Difluoro[1,1′-biphenyl]-3-carboxaldehyde | HCID 46312247 | — |
| Reactant | HCID 82012920 | HCID 82012920 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 89443811 | HCID 89443811 | 85.8% |
Reaction Steps
To a solution of 2-fluoro-5-(3-fluorophenyl)benzaldehyde (505 mg, 2.32 mmol, 1.2 eq) and 2-amino-3-fluoro-6-methoxy-benzonitrile (320 mg, 1.93 mmol, 1 eq) in toluene (30 mL) was added 4 Å molecular sieves (10 g). The mixture was heated at reflux for 4 h, then filtered to remove the molecular sieves. The filtrate was concentrated and the residue obtained was dissolved in methanol (30 mL). NaBH4 (109.6 mg, 2.9 mmol, 1.5 eq) was added and the reaction stirred for 2 h at room temperature. The reaction was quenched by addition of water, and the aqueous layer was extracted with EtOAc. The combined organic extracts were washed with brine, dried (Na2SO4), filtered and evaporated in vacuo. The residue obtained was purified by column chromatography (petroleum ether:EtOAc, 50:1) to give the title compound as an off-white solid (610 mg, 72%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09249085B2 |
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| Source dataset | uspto-grants-2016_02 |
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| ORD ID | ord-88c98a9a917f43eaab3eeb1598336bd9 |
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| Source note | uspto-grants-2016_02 |
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