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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2350994Generated: November 1, 2026

Imidazole → 5-t-Butyldimethylsilyloxy-2-(3-iodopropyl)-4,6,7-trimethyl-1,3-benzoxathiole

https://huagongshe.com/reaction/2350994

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
ReactantWaterHCID 962—
Reactanttert-Butyldimethylsilyl chlorideHCID 28928—
Reactant5-Hydroxy-2-(3-iodopropyl)-4,6,7-trimethyl-1,3-benzoxathioleHCID 13592060—
SolventBenzeneHCID 241—
Product5-t-Butyldimethylsilyloxy-2-(3-iodopropyl)-4,6,7-trimethyl-1,3-benzoxathioleHCID 14802185—

Reaction Conditions

Temperature50 °C

Reaction Steps

5.2 g of t-butyldimethylsilyl chloride and 4.6 g of imidazole were dissolved in 80 ml of benzene, and then the reaction mixture was heated for 1 hour at 50° C., after which a solution of 6.3 g of 5-hydroxy-2-(3-iodopropyl)-4,6,7-trimethyl-1,3-benzoxathiole (prepared as described in Examples 74 and 75) in 10 ml of benzene was added and the reaction mixture was allowed to react for 8 hours at 40°-45° C. The reaction product was cooled, poured into water, and then extracted with benzene. The extract was washed with water and then dried over anhydrous sodium sulfate. The solvent was distilled off under reduced pressure. The resulting residue was subjected to silica gel column chromatography and the title compound was obtained from the fraction eluted with a 9:1 by volume mixture of cyclohexane and benzene.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04871762
Source datasetuspto-grants-1989_10
ORD IDord-76dc0d40ef34427fa255da9570c6245e
Source noteuspto-grants-1989_10