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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 724497Generated: October 25, 2026

HCID 21880924, compound → HCID 21880978, compound

https://huagongshe.com/reaction/724497

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 21880924HCID 21880924—
Reactant(2-Allyloxy-3-tert-butyl-5-methylphenyl)chlorodiethylsilaneHCID 67206735—
ReactantButyllithiumHCID 178418339—
SolventTolueneHCID 1140—
SolventTetrahydrofuranHCID 8028—
ProductHCID 21880978HCID 21880978—

Reaction Steps

At −78° C., n-butyllithium (1.56 M, 1.69 mL, 2.64 mmol) was added dropwise to a solution of 2,5-dimethylcyclopenta[1,2-b:4,3-b′]dithiophen (0.50 g, 2.42 mmol) in tetrahydrofuran (10 mL) and the mixture was stirred at room temperature for 4 hours. After the reaction mixture was cooled to −78° C., a solution of (2-allyloxy-3-tert-buyl-5-methylphenyl)chlorodiethylsilane (0.72 g, 2.20 mmol) in toluene (3 mL) was added dropwise thereto. The resulting reaction mixture was warmed to room temperature and stirred for 2 hours. After the solvent was distilled off under reduced pressure, toluene 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)diethylsilane.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07141690B2
Source datasetuspto-grants-2006_11
ORD IDord-eb56857b284943b4b1889f27cb0c9984
Source noteuspto-grants-2006_11