HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 53811135, compound → HCID 15596444, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 53811135 | HCID 53811135 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Pd barium sulfate | HCID 16218511 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 15596444 | HCID 15596444 | 60.5% |
Reaction Steps
N-Isobutyl-7-phenylhept-2-en-6-ynamide (100 mg) and 5% Pd/BaSO4 (17 ml) in dry methanol (3 ml) at 20° C. was treated with hydrogen until hydrogen uptake was 85% of theoretical. The mixture was diluted with methanol, filtered and the solvent was removed from the filtrate. The residue was treated with ether and the solvent removed in a stream of nitrogen. The product was purified by chromatography on silica (15 g), eluting with 1:1 ether:hexane grading to 100% ether to give N-isobutyl-7-phenylhepta-2E,6Z-dienamide (61 mg) as a yellow oil which crystallised on standing mp 42°-5° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04855086 |
| Source dataset | uspto-grants-1989_08 |
| ORD ID | ord-ca29492cc6f241f48fd41039c8b5ce0e |
| Source note | uspto-grants-1989_08 |