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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1090877Generated: October 31, 2026

Sodium borohydride → (2-Trimethylsilyl-4-furyl)methanol

https://huagongshe.com/reaction/1090877

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant5-(Trimethylsilyl)furan-3-carbaldehydeHCID 15663251—
SolventMethanolHCID 887—
Product(2-Trimethylsilyl-4-furyl)methanolHCID 13333558—

Reaction Steps

2-Trimethylsilyl-4-furaldehyde (1.57 g, 9.35 mmol) was added to a suspension of sodium borohydride (424 mg, 11.2 mmol) in methanol (10 ml) at 0° C. After 45 minutes, most of the methanol was evaporated and the residue taken up in ethyl ether. The ethyl ether extracts were combined, washed (water), dried (magnesium sulfate) and evaporated to dryness to give an oil, which was purified by flash chromotography on silica using 30% ethyl ether/hexane to give the title alcohol as a pale yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05082954
Source datasetuspto-grants-1992_01
ORD IDord-ae4bda673c3849729cb1b87d6b324f55
Source noteuspto-grants-1992_01