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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 569627Generated: October 31, 2026

Imidazole → Silane, [(8-bromooctyl)oxy](1,1-dimethylethyl)dimethyl-

https://huagongshe.com/reaction/569627

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
Reactanttert-Butyldimethylsilyl chlorideHCID 28928—
Reactant1-Octanol, 8-bromo-HCID 162607—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
ProductSilane, [(8-bromooctyl)oxy](1,1-dimethylethyl)dimethyl-HCID 10969362—

Reaction Steps

A solution of dimethyl-t-butylsilyl chloride (18 g.) in tetrahydrofuran (50 ml.) was added dropwise to a stirred solution of 8-bromooctanol (20 g.) and imidazole (14.2 g.) in tetrahydrofuran (100 ml.) and the mixture was stirred at laboratory temperature for 3 hours, diluted with diethyl ether (200 ml.) and filtered. The filtrate was evaporated to dryness and the residue was purified by chromatography on a silica gel column using petroleum ether (b.p. 60°-80° C.) as eluant. A solution of the 8-(dimethyl-t-butylsilyloxy)octyl bromide thus obtained (6.46 g.) in dimethyl sulphoxide (2 ml.) was added to a stirred suspension of lithium acetylide-ethylenediamine complex (2.02 g.) in dimethylsulphoxide (30 ml ) which was cooled to 10° C.; and the mixture was stirred for 18 hours and then poured into ice-water (150 ml.). The mixture was extracted three times with petroleum ether (b.p. 60°-80° C.; 30 ml. each time) and the combined extracts were washed with water (10 ml.), dried and evaporated to dryness. The residue was purified by chromatography on a silica gel column using a 5:1 v/v mixture of cyclohexane and diethyl ether as eluant. There was thus obtained 10-(dimethyl-t-butylsilyloxy)dec-1-yne.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04732912
Source datasetuspto-grants-1988_03
ORD IDord-fde899e7e49c4a47a3fdace45742eef3
Source noteuspto-grants-1988_03