HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,8-Diazabicyclo(5.4.0)undec-7-ene → 1-(2-Benzyloxyphenyl)-4-(3-chlorophenyl)butadiene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,8-Diazabicyclo(5.4.0)undec-7-ene | HCID 81184 | — |
| Reactant | 3-(3-Chlorophenyl)prop-2-enal | HCID 2763111 | — |
| Reactant | 2-Benzyloxybenzyltriphenylphosphonium chloride | HCID 19423967 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 1-(2-Benzyloxyphenyl)-4-(3-chlorophenyl)butadiene | HCID 54522678 | 94% |
Reaction Steps
Following a procedure similar to that described in the first part of Preparation 3, the whole of this 3-(3-chlorophenyl)-2-propenal was reacted with 6.9 g of 2-benzyloxybenzyltriphenylphosphonium chloride (prepared as described in Preparation 1) and 2.89 g of 1,8-diazabicyclo[5,4,0]undec-7-ene in 100 ml of acetonitrile. The crude product, extracted as described in the first part of Preparation 3, was purified as described in the first part of Preparation 3, to give 4.13 g (yield 94%) of 1-(2-benzyloxyphenyl)-4-(3-chlorophenyl)butadiene as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05556864 |
| Source dataset | uspto-grants-1996_09 |
| ORD ID | ord-9d499ca1328845e99ea443d258b77e96 |
| Source note | uspto-grants-1996_09 |