HuagongsheHuagongshe Chemistry Print Report · For research reference only
Carbon Tetrachloride → 4-chloro-1,2-diphenyl-1-[4-[2-(N-methylamino)ethoxy]phenyl]1-butene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Carbon Tetrachloride | HCID 5943 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | (Z)-1,2-diphenyl-1-[4-[2-(N-methylamino)ethoxy]phenyl]-1-buten-4-ol hydrochloride | HCID 67944775 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 4-chloro-1,2-diphenyl-1-[4-[2-(N-methylamino)ethoxy]phenyl]1-butene | HCID 119344 | — |
Reaction Steps
A mixture containing 41.0 g of (Z)-1,2-diphenyl-1-[4-[2-(N-methylamino)ethoxy]phenyl]-1-buten-4-ol hydrochloride, 57.4 g of triphenyl phosphine, 61.6 g of carbon tetrachloride and 500 ml of acetonitrile is refluxed for 1 h. On cooling the product crystallizes out and is collected for filtration. The yield of the hydrochloride is 25.3 g (59%) and m.p. 206°-8° C. The base is liberated from its salt by conventional means giving an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04996225 |
| Source dataset | uspto-grants-1991_02 |
| ORD ID | ord-c61b0e4e795d4aa1bb539ba9ef93b869 |
| Source note | uspto-grants-1991_02 |