HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → HCID 21914400, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | p-Bromoacetophenone | HCID 7466 | — |
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Catalyst | Titanium isopropoxide | HCID 11026 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 21914400 | HCID 21914400 | — |
Reaction Steps
4-Bromoacetophenone (1.95 g), piperidine (0.97 ml) and titanium(IV) isopropoxide (3.64 ml) were stirred under argon at room temperature for 1 h. Ethanol (10 ml) was added, followed by sodium cyanoborohydride (0.41 g) and mixture stirred for 18 h. Water (2 ml) was then added and the mixture stirred for 20 minutes. The resulting inorganic precipitate was filtered off, washed with ethanol (20 ml) and the combined organic phase was concentrated in vacuo, redissolved in toluene and purified by Bondelute® chromotography, eluting with 0–20% ethyl acetate/iso-hexane to give the product as a pale yellow oil (1.07 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07125896B2 |
| Source dataset | uspto-grants-2006_10 |
| ORD ID | ord-216b0b8ea209470ebda97b9986151d62 |
| Source note | uspto-grants-2006_10 |