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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 556131Generated: October 30, 2026

Toluene → HCID 131729269, compound

https://huagongshe.com/reaction/556131

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 131729268HCID 131729268—
SolventDichloromethaneHCID 6344—
ProductHCID 131729269HCID 1317292696%

Reaction Conditions

Temperature80 °C

Reaction Steps

Firstly, dist. toluene (5 mL) was added to and dissolved in 1-(diallylethoxysilyl)-4-(3,5-dimethyl-3-hydroxy-hexynyl)benzene (125 mg, 0.35 mmol) obtained in Synthesis example 10. The resultant mixture was added with NaOH (9.9 mg, 0.25 mmol), and then was stirred under a nitrogen atmosphere at 80° C. for 16 hours to obtain a reaction mixture. Then, the reaction mixture was diluted with CH2Cl2, and an organic layer was washed with dist. H2O and sat. NaCl. The organic layer thus collected was dried with MgSO4, and the dried organic layer was filtered and concentrated to obtain a crude product. The obtained crude product was separated and purified by silica gel column chromatography (hexane/EtOAc=5/1) to obtain 1-(diallylethoxysilyl)-4-ethynylbenzene (5 mg, 6% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08053588B2
Source datasetuspto-grants-2011_11
ORD IDord-b5e00d7f33c646e7a88cc0beb97ee03f
Source noteuspto-grants-2011_11