HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1497450Generated: October 30, 2026
Sodium borohydride → HCID 86680621, compound
https://huagongshe.com/reaction/1497450
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 86680620 | HCID 86680620 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 86680621 | HCID 86680621 | 73.7% |
Reaction Steps
To a solution of 1-(5-(furan-3-yl)pyridin-2-yl)ethanone (0.2 g, 1.0752 mmol) in MeOH (10 ml) was added sodium borohydride (0.0795 g, 2.150 mmol) at 0° C., the reaction mixture warmed to room temperature and was stirred for 2 h. The reaction mixture was evaporated under reduced pressure to remove the methanol, diluted with water (15 mL), extracted with ethyl acetate (200 mL), dried over sodium sulphate and concentrated under reduced pressure to obtain crude product. The crude product was purified by Biotage Isolera® One column (using 20% ethyl acetate and hexane to give 1-(5-(furan-3-yl)pyridin-2-yl)ethanol as a colorless liquid (0.150 g, 73% yield). 1H NMR (400 MHz, DMSO-d6): δ 8.68 (s, 1H), 7.76 (t, 2H), 7.52 (s, 1H); 7.28 (t, 1H), 6.71 (s, 1H), 4.91 (d, 1H), 4.14-4.07 (m, 1H), 1.52 (d, 3H): LC-MS m/z calcd for [M+H]+ 189.08. found 190.0.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09199975B2 |
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| Source dataset | uspto-grants-2015_12 |
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| ORD ID | ord-23008e35833441b994b4866fddb7fb60 |
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| Source note | uspto-grants-2015_12 |
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