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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1497450Generated: October 30, 2026

Sodium borohydride → HCID 86680621, compound

https://huagongshe.com/reaction/1497450

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 86680620HCID 86680620—
SolventMethanolHCID 887—
ProductHCID 86680621HCID 8668062173.7%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09199975B2
Source datasetuspto-grants-2015_12
ORD IDord-23008e35833441b994b4866fddb7fb60
Source noteuspto-grants-2015_12