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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1197725Generated: October 26, 2026

Trimethylsilane → 4-(1-Trimethylsilylhexyloxy)phenyl 4-(1-trimethylsilylbutyloxy)benzoate

https://huagongshe.com/reaction/1197725

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethylsilaneHCID 70435—
Reactant4-(5-Hexenyloxy)phenyl 4-(3-butenyloxy)benzoateHCID 19972137—
CatalystHCID 178479810HCID 178479810—
SolventDichloromethaneHCID 6344—
Product4-(1-Trimethylsilylhexyloxy)phenyl 4-(1-trimethylsilylbutyloxy)benzoateHCID 19104494—

Reaction Steps

0.35 g (0.01 mmol of Pt) of L.5% strength dicyclopentadienylplatinum dichloride solution in dichloromethane was added as catalyst to a solution of 5.00 g (9.71 mmol) of 4-(5-hexenyloxy)phenyl 4-(3-butenyloxy)benzoate in 10 ml of dichloromethane, and 2.02 g (27.2 mmol) of trimethylsilane were passed into the refluxing mixture over the course of 8 hours. After complete hydrosilylation of the olefin, the reaction mixture was flushed with nitrogen, and the dichloromethane was removed by vacuum distillation on a rotary evaporator. The crude product was purified by chromatography on silica gel, to give 4-(1-trimethylsilylhexyloxy)phenyl 4-(1-trimethylsilylbutyloxy)benzoate, phases: c 72 i.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05277838
Source datasetuspto-grants-1994_01
ORD IDord-e2f6d6b83bba4bdf8f1698a3c647b36a
Source noteuspto-grants-1994_01