HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1669231Generated: October 30, 2026
Sodium borohydride → HCID 59729431, compound
https://huagongshe.com/reaction/1669231
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | Ethyl acetate hexane | HCID 21226206 | — |
| Reactant | HCID 59729402 | HCID 59729402 | — |
| Solvent | MeOH tetrahydrofuran | HCID 21899815 | — |
| Product | HCID 59729431 | HCID 59729431 | 100.4% |
Reaction Steps
To a 0° C. solution of (3-fluoro-4′-trifluoromethyl-biphenyl-4-yl)-acetaldehyde (372 mg, 1.31 mmol) in THF/MeOH (10/3 mL) is added portion-wise sodium borohydride (100 mg, 2.62 mmol) and warmed to room temperature. After 1 h TLC (30% EtOAc/hexane) indicates complete consumption of starting material. The reaction mixture is concentrated and the residue is partitioned between EtOAc (100 mL) and 0.2N HCl (20 mL). The aqueous layer is extracted with a second portion of EtOAc (50 mL). The combined organic layers are washed with brine, dried (MgSO4), filtered and concentrated to yield the title compound (374 mg, quant.). 1NMR (400 MHz, CDCl3) δ ppm: 7.68 (q, 4H, J=8.2 Hz), 7.38-7.32 (m, 2H), 7.29 (d, 1H, J=11.0 Hz), 3.92 (t, 2H, J=6.6 Hz), 2.97 (t, 2H, J=6.6 Hz).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07989457B2 |
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| Source dataset | uspto-grants-2011_08 |
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| ORD ID | ord-62e009aa590e4a5f864cb489178d023e |
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| Source note | uspto-grants-2011_08 |
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