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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 29460Generated: October 27, 2026

Tetrahydrofuran → 1-Benzofuran-2-Ylmethanol

https://huagongshe.com/reaction/29460

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
Reactant2-BenzofurancarboxaldehydeHCID 61341—
ReactantSodium borohydrideHCID 4311764—
SolventMethanolHCID 887—
Product1-Benzofuran-2-YlmethanolHCID 2776263—

Reaction Steps

To benzofuran-2-carbaldehyde (4 g, 27.4 mmol, 1 eq.), THF (50 mL) and methanol (50 mL) were added, under argon, and the reaction was cooled using an ice-salt bath. Then sodium borohydride (3.11 g, 82.1 mmol, 3 eq.) was added in several portions, and the reaction was allowed to warm slowly to room temperature for 1 hour. After work-up, benzofuran-2-yl-methanol was obtained in quantitative yield. 1H NMR (400 MHz, DMSO-d6) δ ppm 4.6 (d, J=5.8 Hz, 2 H) 5.5 (t, J=5.9 Hz, 1 H) 6.8 (s, 1 H) 7.3 (m, 2 H) 7.6 (m, 2 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07420001B2
Source datasetuspto-grants-2008_09
ORD IDord-1e582aff1d874a949b42c9d479715f19
Source noteuspto-grants-2008_09