HuagongsheHuagongshe Chemistry Print Report · For research reference only
3,3-Diphenylacrolein → Ethyl 4-(4-(3,3-diphenylallyl)piperazin-1-yl)benzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3,3-Diphenylacrolein | HCID 71027 | — |
| Reactant | Cyano-borohydride | HCID 498716 | — |
| Reactant | Ethyl 4-(piperazin-1-yl)benzoate | HCID 2761178 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Ethyl 4-(4-(3,3-diphenylallyl)piperazin-1-yl)benzoate | HCID 67144443 | — |
Reaction Steps
A suspension of ethyl 4-piperazin-1-ylbenzoate (1.36 g) and 3,3-diphenylacrylaldehyde (1.56 g) in dichloromethane (10 mL) and methanol (10 mL) was treated with polymer-supported cyanoborohydride (2.47 mmol/g, 6 g), shaken at room temperature for 24 hours, and filtered. The resin was washed with 1:1 dichloromethane/methanol (10 mL×3) and the combined filtrates were concentrated. The concentrate was purified by silica gel chromatography eluting with a gradient from 10%-50% ethyl acetate/hexanes to provide the desired product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08338466B2 |
| Source dataset | uspto-grants-2012_12 |
| ORD ID | ord-7f3359281e5049e2a89d09c8314406e4 |
| Source note | uspto-grants-2012_12 |