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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2050547Generated: November 2, 2026

((4-(tert-Butyl)phenyl)ethynyl)trimethylsilane → Trimethylsilyl[4-(4-methylpentyl)]phenylethyne

https://huagongshe.com/reaction/2050547

Reaction equation

Participants

RoleNameHCIDCharge
Reactant((4-(tert-Butyl)phenyl)ethynyl)trimethylsilaneHCID 14989664—
Reactant4-(4-Methylpentyl)bromobenzeneHCID 22409093—
ProductTrimethylsilyl[4-(4-methylpentyl)]phenylethyneHCID 54327813—

Reaction Steps

Using the same general procedure as described for Compound 21, but using instead 4-(4-methylpentyl) bromobenzene (Compound 30), the title compound was synthesized as a colorless oil. PMR (CDCl3): & 0.32 (9H, s), 0.93 (6H, d, J~6.6 Hz), 1.18-1.29 (2H, m), 1.52-1.70 (3H, m), 2.58 (2H, t, J~7.7 Hz), 7.12 (2H, d, J~8.1 Hz), 7.43 (2H, d, J~8.1 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05013744
Source datasetuspto-grants-1991_05
ORD IDord-06c25c6d5c69460d9a48df33cecaec16
Source noteuspto-grants-1991_05