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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 432083Generated: October 25, 2026

Imidazole → tert-butyl(dimethyl)silyl [(2R)-6-iodo-3,4-dihydro-2H-chromen-2-yl]methyl ether

https://huagongshe.com/reaction/432083

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
ReactantWaterHCID 962—
Reactanttert-Butyldimethylsilyl chlorideHCID 28928—
Reactant[(2R)-6-iodo-3,4-dihydro-2H-chromen-2-yl]methanolHCID 9943850—
SolventDimethylformamideHCID 6228—
Producttert-butyl(dimethyl)silyl [(2R)-6-iodo-3,4-dihydro-2H-chromen-2-yl]methyl etherHCID 1027255279%

Reaction Conditions

Temperature27 °C

Reaction Steps

A reaction mixture containing [(2R)-6-iodo-3,4-dihydro-2H-chromen-2-yl]methanol (Example 8, 5 g, 17.2 mmol, 1.0 eq), tert-butyldimethylsilyl chloride (20.6 mmol, 1.2 eq), and imidazole (43 mmol, 2.5 eq) in anhydrous DMF (35 mL) was stirred at 27° C. overnight. The resulting mixture was then cooled to room temperature, poured into water, and extracted with diethyl ether. The organic extract was washed with water, brine, dried over anhydrous sodium sulfate, concentrated, and purified by medium pressure column chromatography (Biotage 40S normal phase silica gel column) providing the product in 79% yield; m/z=405 [MH=].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06660752B2
Source datasetuspto-grants-2003_12
ORD IDord-7e3f16864e7948d4bc674023bef49cce
Source noteuspto-grants-2003_12