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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 334724Generated: October 30, 2026

Hexane → 7-chloro-1-methyl-2-(4-(trimethylsilyl)but-3-ynyl)-1H-benzo[d]imidazole

https://huagongshe.com/reaction/334724

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexaneHCID 8058—
Reactant1-(Trimethylsilyl)prop-1-yneHCID 80363—
Reactant7-chloro-2-(chloromethyl)-1-methyl-1H-benzo[d]imidazoleHCID 43659927—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product7-chloro-1-methyl-2-(4-(trimethylsilyl)but-3-ynyl)-1H-benzo[d]imidazoleHCID 66598391100%

Reaction Steps

To a solution of the trimethyl(prop-1-ynyl)silane (0.21 mL, 1.4 mmol) in THF (4 mL), was added at −78° C. nBuLi 2.5M in hexane (0.56 mL, 1.3 mmol). After 90 min at −78° C., a solution of 7-chloro-2-(chloromethyl)-1-methyl-1H-benzo[d]imidazole (250 mg, 1.2 mmol) in THF (2 mL) was added. Mixture went from purple to orange and then dark brown. The reaction was quenched after 1 h at −78° C. with water and the solvent was evaporated to dryness to afford 338 mg of 7-chloro-1-methyl-2-(4-(trimethylsilyl)but-3-ynyl)-1H-benzo[d]imidazole (Yield: 100%) as a brown oily solid. It was carried through to the next step without purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08883826B2
Source datasetuspto-grants-2014_11
ORD IDord-aaef67279c114c3997882e47df318479
Source noteuspto-grants-2014_11