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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2247835Generated: November 2, 2026

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

https://huagongshe.com/reaction/2247835

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 (Compound 22) (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 numberUS05037811
Source datasetuspto-grants-1991_08
ORD IDord-677a2e92e08f41e49a9aa1ee7069a77f
Source noteuspto-grants-1991_08