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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hexane | HCID 8058 | — |
| Reactant | 1-Hexyne | HCID 12732 | — |
| Reactant | Chloro(chloromethyl)[bis(4-fluorophenyl)]silane | HCID 13392398 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Chloromethyl[bis(4-fluorophenyl)](1-hexynyl)silane | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04530922 |
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| Source dataset | uspto-grants-1985_07 |
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| ORD ID | ord-c2776b6f5b26486eb8fcccc544e29e1f |
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| Source note | uspto-grants-1985_07 |
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