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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2274455Generated: October 30, 2026

Methanol → HCID 21911993, compound

https://huagongshe.com/reaction/2274455

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantTosylmethyl isocyanideHCID 161915—
Reactant1-((2-(trimethylsilyl)ethoxy)methyl)-1H-imidazole-2-carbaldehydeHCID 13600235—
ReactantPotassium tert-butoxideHCID 23665647—
SolventWaterHCID 962—
Solvent1,2-DimethoxyethaneHCID 8071—
ProductHCID 21911993HCID 219119934,151.6%

Reaction Conditions

Temperature-60 °C

Reaction Steps

1.73 g (8.84 mmol) tosylmethylisocyanide were solved in 10 ml DME and cooled down to −60° C. At this temperature first 1.98 g potassium tert-butoxide was added then slowly a solution of 2.00 g (8.84 mmol) 1-(2-trimethylsilanyl-ethoxymethyl)-1H-imidazole-2-carbaldehyde in 5 ml DME. After 2 hours stirring at −60° C. the reaction was allowed to reach 0° C. and 5 ml methanol (123.60 mmol) was added to the solution. The reaction was stirred for further 24 hours at ambient temperature and for 2 hours at 40° C. Excess water was added and the solution was extracted 3 times with dichloromethane. The organic phase was dried over Na2SO4, after evaporation of the solvent under reduced pressure the raw material was purified by reverse phase column chromatography (water 0.1% TFA/acetonitrile=80/20 to yield 0.87 g (0.367 mol) of the SEM-protected imidazole-acetonitrile.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09126972B2
Source datasetuspto-grants-2015_09
ORD IDord-e74c688bfbb3465b80b7e367a16d937c
Source noteuspto-grants-2015_09