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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 326774Generated: October 30, 2026

1-((2-(trimethylsilyl)ethoxy)methyl)-1H-imidazole-2-carbaldehyde → (1-((2-(trimethylsilyl)ethoxy)methyl)-1H-imidazol-2-yl)methanol

https://huagongshe.com/reaction/326774

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-((2-(trimethylsilyl)ethoxy)methyl)-1H-imidazole-2-carbaldehydeHCID 13600235—
ReactantAluminium lithium hydrideHCID 21226445—
SolventDiethyl EtherHCID 3283—
Product(1-((2-(trimethylsilyl)ethoxy)methyl)-1H-imidazol-2-yl)methanolHCID 2187760089.6%

Reaction Steps

A solution of 1-[[2-(trimethylsilyl)ethoxy]methyl]-1H-imidazole-2-carboxaldehyde (prepared according to procedures described by J. P. Whitten et al., J. Org. Chem., 51 (1986), 1891) (9.95 g, 44.0 mmol) in dry ether (40 ml) was dropped into a suspension of lithium aluminum hydride (0.42 g, 12.0 mmol) in dry ether (40 ml) and stirring was continued for 4 hours at room temperature. Then ice-water was added carefully, and the precipitated aluminum hydroxide was filtered off and washed with ether. The aqueous phase was separated and the organic phase was washed with water, dried over sodium sulfate an evaporated in vacuo to leave an oil (9.0 g) which crystallized spontaneously. Yield: 7.1 g, m.p. 68°-69° C. (from pentane).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05270334
Source datasetuspto-grants-1993_12
ORD IDord-550deb02136e4a33927e2fb8b40d58a3
Source noteuspto-grants-1993_12