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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1620146Generated: October 30, 2026

Dibenzo(b,d)furan-2-carboxaldehyde → 2-Dibenzofuranmethanol

https://huagongshe.com/reaction/1620146

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDibenzo(b,d)furan-2-carboxaldehydeHCID 220843—
ReactantSodium borohydrideHCID 4311764—
SolventTetrahydrofuranHCID 8028—
Product2-DibenzofuranmethanolHCID 290846—

Reaction Steps

To a solution of dibenzo[b,d]furan-2-carbaldehyde (191 mg, 973 μmol) in THF (10 mL) in a 50 mL round-bottomed flask equipped with a magnetic stirrer was added NaBH4 (37 mg, 0.978 mmol) and the mixture was stirred for 2 h at RT and quenched by adding 10 mL of a 1 N aq. HCl solution. The reaction mixture was stirred at RT for 20 min and extracted with CH2Cl2 (2×50 mL). The organic phase was washed with water (10 mL), brine (10 mL), dried over Na2SO4, filtered and concentrated at 40° C. under vacuum to afford dibenzo[b,d]furan-2-ylmethanol CCH 34116 as an off-white solid (192 mg, 100% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08772316B2
Source datasetuspto-grants-2014_07
ORD IDord-b27249f368fd40b18b28f1140564a95c
Source noteuspto-grants-2014_07