HuagongsheHuagongshe Chemistry Print Report · For research reference only
3,3-Diphenylacrolein → 4-(4-(3,3-Diphenyl-2-propenyl)-1-piperazinyl)benzonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3,3-Diphenylacrolein | HCID 71027 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Cyano-borohydride | HCID 498716 | — |
| Reactant | 4-(Piperazin-1-yl)benzonitrile hydrochloride | HCID 2733994 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-(4-(3,3-Diphenyl-2-propenyl)-1-piperazinyl)benzonitrile | HCID 59186611 | 84.3% |
Reaction Steps
A suspension of 4-piperazin-1-ylbenzonitrile hydrochloride (1.30 g, 5.00 mmol) and 3,3-diphenylacrylaldehyde (1.56 g, 7.50 mmol)) in dichloromethane (10 mL) and methanol (10 mL) was neutralized to pH 5 with diisopropylethylamine, treated with polymer-supported cyanoborohydride (2.47 mmol/g, 6 g, 14.82 mmol), 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 (1.60 g, 84%). MS (CI) m/e 380 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07585858B2 |
| Source dataset | uspto-grants-2009_09 |
| ORD ID | ord-0b4095b6d8be45d7a5f7dc22995109e0 |
| Source note | uspto-grants-2009_09 |