HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetaldehyde → 81244-91-9
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetaldehyde | HCID 177 | — |
| Reactant | HCID 22813385 | HCID 22813385 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 81244-91-9 | HCID 14254830 | 58.5% |
Reaction Steps
A suspension of trans-4,6,6a,8,9,10a-hexahydro-7H-indolo-[3,4 gh]-[1,4]-benzoxazine (650 mg, 0.03 m) acetaldehyde (260 mg, 0.006 m) and Pd/c (10%, 700 mg) in abs. ethanol (50 ml) is hydrogenated at room temperature for 4 hours. The catalyst is removed by filtration, and the solvent is removed under reduced pressure (20 mm). The oil is recrystallized from methanol to yield 430 mg of trans 4,6,6a,8,9,10a-hexahydro-7-ethyl-7H-indolo-[3,4 gh]-[1,4]benzoxazine, m.p. turns brown 200° melt 210°-213°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04238486 |
| Source dataset | uspto-grants-1980_12 |
| ORD ID | ord-06e7e7f5280f4cf08c69511a09a0f74a |
| Source note | uspto-grants-1980_12 |