HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,1,1-Trichloroethane → HCID 86743115, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,1,1-Trichloroethane | HCID 6278 | — |
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | HCID 54242499 | HCID 54242499 | — |
| Product | HCID 86743115 | HCID 86743115 | — |
Reaction Steps
A mixture of 3.8 g (0.01 mol) of bis(4-acetoxyphenyl)phenylphosphine, 1.7 g (0.01 mol) of α-bromotoluene and 15 ml of 1,1,1-trichloroethane was heated to reflux at which time complete solution was achieved. Shortly thereafter, product began to precipitate from solution. After heating at reflux for 2.5 hr, the mixture was cooled, filtered and the solid was washed with ether and dried. The yield of benzylbis(4-acetoxyphenyl)phenylphosphonium bromide was 5.0 g (90.0% of theory); mp=233°-5° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04837394 |
| Source dataset | uspto-grants-1989_06 |
| ORD ID | ord-4e46fe4409c14bcda2d8b4d16ffe3de5 |
| Source note | uspto-grants-1989_06 |