HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 68696410, compound → HCID 17993212, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 68696410 | HCID 68696410 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 17993212 | HCID 17993212 | 185.5% |
| Product | HCID 68696410 | HCID 68696410 | — |
Reaction Steps
To a suspension of 10% palladium on carbon (200 mg) in absolute ethanol (30 mL) was added a solution of (2E)-3-(1H-indol-4-yl)prop-2-en-1-ol (0.98 g, 5.66 mmol) in ethyl acetate (30 mL) and the mixture hydrogenated at 50 psi for 15 min. The reaction mixture was filtered through celite and concentrated in vacuo to give a light purple syrup. (2E)-3-(1H-indol-4-yl)prop-2-en-1-ol was prepared by the method of Kardos, N.; Genet J-P. Tetrahedron Asymmetry 1994, 5, 1525-1533, which is incorporated herein by reference in its entirety. Purification by flash chromatography (20% to 50% ethyl acetate/hexane) gave the title compound as a colorless syrup (0.92 g, 93%). MS (ES+) m/z 176.2 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07645752B2 |
| Source dataset | uspto-grants-2010_01 |
| ORD ID | ord-dff3d954f9724f918526dca278fbf08e |
| Source note | uspto-grants-2010_01 |