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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 371309Generated: October 27, 2026

Hexane → Chloromethyl[bis(4-fluorophenyl)](1-hexynyl)silane

https://huagongshe.com/reaction/371309

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexaneHCID 8058—
Reactant1-HexyneHCID 12732—
ReactantChloro(chloromethyl)[bis(4-fluorophenyl)]silaneHCID 13392398—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductChloromethyl[bis(4-fluorophenyl)](1-hexynyl)silaneHCID 20273717—

Reaction Steps

A solution of 2.9 ml (0.024 mol) of 1-hexyne in 50 ml of tetrahydrofuran under nitrogen was cooled to -5° C. A solution of n-butyllithium in hexane (15 ml of 1.6 molar, 0.024 mol) was added dropwise, and the resulting solution was warmed to room temperature and stirred for 1.5 hours. The solution was then cooled to -65° C., and a solution of 6.0 g (0.0198 mol) of bis(4-fluorophenyl)chlorochloromethylsilane in 10 ml of THF was added dropwise. The reaction was warmed to room temperature and quenched by addition of saturated aqueous ammonium chloride. The solution was partitioned between water and ether, and the organic layer was separated, washed with brine and dried over magnesium sulfate. Removal of solvent gave the title compound as a clear colorless oil: nmr (CDCl3) 1.0 (3H, m), 1.5 (4H, m), 2.4 (2H, m), 3.2 (2H, s), 7.2 (4H, t, J= 9 Hz), 7.7 (4H, d of d, J=9, 6 Hz); ir (neat) 2180 cm-1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04530922
Source datasetuspto-grants-1985_07
ORD IDord-c2776b6f5b26486eb8fcccc544e29e1f
Source noteuspto-grants-1985_07