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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 326375Generated: October 29, 2026

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

https://huagongshe.com/reaction/326375

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 numberUS05268387
Source datasetuspto-grants-1993_12
ORD IDord-4c3b68022e4140e9b71f8f1fff530767
Source noteuspto-grants-1993_12