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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1295485Generated: October 31, 2026

(2-Allyloxy-3-tert-butyl-5-methylphenyl)chlorodimethylsilane → (2-Allyloxy-3-tert-butyl-5-methylphenyl)(2,5-dimethylcyclopenta[1,2-b:4,3-b']dithiophen-7-yl)dimethylsilane

https://huagongshe.com/reaction/1295485

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(2-Allyloxy-3-tert-butyl-5-methylphenyl)chlorodimethylsilaneHCID 21880918—
ReactantHCID 178506637HCID 178506637—
SolventTolueneHCID 1140—
SolventTetrahydrofuranHCID 8028—
Product(2-Allyloxy-3-tert-butyl-5-methylphenyl)(2,5-dimethylcyclopenta[1,2-b:4,3-b']dithiophen-7-yl)dimethylsilaneHCID 21881029—

Reaction Steps

A solution of (2-allyloxy-3-tert-buyl-5-methylphenyl)chlorodimethylsilane (0.71 g, 2.40 mmol) in toluene (4 mL) was added dropwise to a solution of (2,5-dimethylcyclopenta[1,2-b:4,3-b′]dithiophen-7-yl)lithium (0.51 g, 2.40 mmol) in tetrahydrofuran (10 mL) at −78° C. The resulting reaction mixture was warmed to room temperature and stirred for 5 hours. After the solvent was distilled off under reduced pressure, hexane was added and the mixture was filtered to remove insoluble substances. The filtrate was concentrated under reduced pressure to quantitatively obtain (2-allyloxy-3-tert-butyl-5-methylphenyl)(2,5-dimethylcyclopenta[1,2-b:4,3-b′]dithiophen-7-yl)dimethylsilane.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07241927B2
Source datasetuspto-grants-2007_07
ORD IDord-6b1efef458d047da8641283417d3dd67
Source noteuspto-grants-2007_07