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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1189267Generated: October 25, 2026

1-(Trimethylsilyl)prop-1-yne → 1-benzyl-2-(4-(trimethylsilyl)but-3-ynyl)-1H-benzo[d]imidazole

https://huagongshe.com/reaction/1189267

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(Trimethylsilyl)prop-1-yneHCID 80363—
Reactant1-Benzyl-2-chloromethyl-1H-benzoimidazoleHCID 563436—
Product1-benzyl-2-(4-(trimethylsilyl)but-3-ynyl)-1H-benzo[d]imidazoleHCID 66598005102.4%

Reaction Steps

The title compound was prepared in accordance with the general method of Example 191(D), from of 1-benzyl-2-(chloromethyl)-1H-benzo[d]imidazole (500 mg, 1.9 mmol) and trimethyl(prop-1-ynyl)silane (262 mg, 2.34 mmol). 1-benzyl-2-(4-(trimethylsilyl)but-3-ynyl)-1H-benzo[d]imidazole (647 mg, Yield: 100%) was obtained as a brown oil which was used in the next step without purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08674106B2
Source datasetuspto-grants-2014_03
ORD IDord-c82c574a8a8e47a6bab3b3414f206a28
Source noteuspto-grants-2014_03