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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 36353Generated: October 25, 2026

1-Bromo-3-tert-butylbenzene → (3-tert-Butyl-phenylethynyl)-trimethyl-silane

https://huagongshe.com/reaction/36353

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Bromo-3-tert-butylbenzeneHCID 343798—
Reactant((4-(tert-Butyl)phenyl)ethynyl)trimethylsilaneHCID 14989664—
Product(3-tert-Butyl-phenylethynyl)-trimethyl-silaneHCID 14989665—

Reaction Steps

Using the same general procedure as described for Compound 21, but using 3-tert-butyl-bromobenzene, (Compound 24) the title compound was synthesized as a colorless oil. PMR (CDCl3): & 0.36 (9H, s), 1.40 (9H, s), 7.32 (1H, m), 7.37-7.47 (2H, m), 7.61 (1H, m).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05414007
Source datasetuspto-grants-1995_05
ORD IDord-93172ea14d014b5082f9ac3dba64bfad
Source noteuspto-grants-1995_05