Isopropanol → Chloro(chloromethyl)[bis(4-fluorophenyl)]silane

A suspension of 7.0 g (0.288 mol) of magnesium turnings in 50 ml of ether was stirred under nitrogen while a solution of 50.2 g (0.287 mol) of 4-bromofluorobenzene in 200 ml of ether was added dropwise at a rate that maintained gentle reflux. After another 2 hours at reflux, the mixture was chilled in ice and a solution of 12.0 ml (0.096 mol) of chloromethyltrichlorosilane in 30 ml of ether was added dropwise. The resulting mixture was refluxed for 4 hours, chilled in ice, treated with a solution of 7.5 ml of isopropanol in 20 ml of ether, stirred 5 minutes, and filtered. The filtrate was evaporated to leave a viscous oil that was stirred with hexanes to give a slurry. Filtration under nitrogen and evaporation of the filtrate left a mobile oil that was distilled to give 17.6 g (61%) of the title compound: bp 100°-140° (0.1 mm); nmr (CDCl3) 3.3 (2H, s), 7.1 (4H, t), 7.7 (4H, d of d).

1. additionwas added dropwise at a rate that
2. temperaturemaintained gentle reflux
3. temperatureAfter another 2 hours at reflux
4. temperaturethe mixture was chilled in ice
5. temperatureThe resulting mixture was refluxed for 4 hours
6. temperaturechilled in ice
7. filtrationfiltered
8. customThe filtrate was evaporated
9. customto leave a viscous oil that
10. customto give a slurry
11. filtrationFiltration under nitrogen
12. customevaporation of the filtrate
13. waitleft a mobile oil that
14. distillationwas distilled

ORDレコード

ord-2bf285dc180946349040e574b47bfa9c

出典データセット

uspto-grants-1985_04

DOI

10.6084/m9.figshare.5104873.v1

特許番号

US04510136