HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1472885Generated: October 29, 2026
Sodium borohydride → HCID 86671310, compound
https://huagongshe.com/reaction/1472885
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | D-Valinol | HCID 6950587 | — |
| Reactant | 6-Bromo-3-fluoropyridine-2-carbaldehyde | HCID 16414238 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 86671310 | HCID 86671310 | — |
Reaction Steps
6-bromo-3-fluoropicolinaldehyde (4.0 g, 19.61 mmol) and (R)-2-amino-3-methylbutan-1-ol (2.281 mL, 20.59 mmol) were dissolved in methanol (100 mL) and stirred at ambient temperature for 1 hour and 15 minutes. Sodium borohydride (0.742 g, 19.61 mmol) was added and the mixture was stirred for another 1 hour and 30 minutes. The volume of the reaction mixture was reduced, and the mixture was quenched with 200 mL 1.0 N NaOH, and extracted with 200 mL dichloromethane (2×). The organic phase was extracted with 1.0 N HCl and partitioned. The aqueous phase was separated, neutralized with 3.0 N NaOH, extracted with EtOAc, organic phase separated and washed with brine. The organic phase was dried over Na2SO4, filtered, and concentrated to obtain the title compound as an orange solid. MS (ESI+) m/z 291.0 (M+H); 1H NMR (300 MHz, DMSO-d6) δ 7.69 (t, J=8.8, 1H), 7.60 (dd, J=8.6, 3.7, 1H), 4.42 (t, J=5.2, 1H), 3.92-3.75 (m, 2H), 3.43 (dt, J=10.7, 4.8, 1H), 2.34-2.24 (m, 1H), 2.08 (s, 1H), 1.87-1.71 (m, 1H), 0.83 (dd, J=8.5, 6.9, 6H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09012651B2 |
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| Source dataset | uspto-grants-2015_04 |
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| ORD ID | ord-b1dcafa51aa940f09838f82798b8ccf3 |
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| Source note | uspto-grants-2015_04 |
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