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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1109857Generated: November 2, 2026

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

https://huagongshe.com/reaction/1109857

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 numberUS05322953
Source datasetuspto-grants-1994_06
ORD IDord-ba358602e5c34e3aba8829e61344e909
Source noteuspto-grants-1994_06