HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trichloro(chloromethyl)silane → Silane, dichloro(chloromethyl)phenyl-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trichloro(chloromethyl)silane | HCID 15258 | — |
| Reactant | HCID 178506676 | HCID 178506676 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Silane, dichloro(chloromethyl)phenyl- | HCID 12747007 | 29% |
Reaction Steps
A solution of 25.1 ml (36.8 g, 0.200 mol) of chloromethyltrichlorosilane in 400 ml dry tetrahydrofuran was cooled to -78° under nitrogen and stirred vigorously while 48.0 ml (0.100 mol) of 2.1 molar phenyllithium was slowly dripped in over 1 hour. After stirring another 30 minutes at -78° the solution was allowed to warm to room temperature and evaporated to about 200 ml. Addition of 500 ml ether, filtration to remove precipitated lithium chloride, and evaporation of the filtrate left 25.0 g of liquid. Distillation gave 6.5 g (29%) of the title compound as a colorless liquid: bp 62°-82° (0.15 mm); nmr (CDCl3): δ3.3 (s, 2) and 7.1-7.9 (m, 5).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04510136 |
| Source dataset | uspto-grants-1985_04 |
| ORD ID | ord-c3753a67601a481f8f676519bccbe353 |
| Source note | uspto-grants-1985_04 |