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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2101461Generated: October 30, 2026

Sodium borohydride → HCID 22591563, compound

https://huagongshe.com/reaction/2101461

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant5-Chloro-3-methyl-1-benzofuran-2-carbaldehydeHCID 4736982—
SolventEthanolHCID 702—
ProductHCID 22591563HCID 2259156388.4%

Reaction Steps

To a solution of 5-chloro-3-methyl benzofuran-2-carboxaldehyde (5.55 mmol, 1.08 g) in ethanol (25 mL) was added portion-wise sodium borohydride (16.6 mmol, 630 mg). After one hour, the ethanol was evaporated and the residue was partitioned between CHCl3 and H2O. The CHCl3 layer was collected, filtered, dried, and evaporated to dryness to obtain 5-chloro-3-methyl benzofuran 2-methanol (88%, 965 mg); mp 112° C.-113° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07572910B2
Source datasetuspto-grants-2009_08
ORD IDord-e4ada1751f8c4128af6418c915df0196
Source noteuspto-grants-2009_08