HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Benzyloxyphenylacetaldehyde → HCID 23322068, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Benzyloxyphenylacetaldehyde | HCID 11413489 | — |
| Reactant | 4-Aminoethyl-2(3H)-indolone | HCID 23322037 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 23322068 | HCID 23322068 | — |
Reaction Steps
A mixture of 0.9 g of 4-(2-aminoethyl)-2(3H)-indolone, 0.23 g of 4-benzyloxyphenylacetaldehyde, 0.25 g of 10% palladium-on-charcoal and 100 ml of ethanol is hydrogenated at 50 p.s.i. at 50° until the uptake of hydrogen is complete. After filtration, the mother liquors are evaporated to give 4-[2-(4-hydroxyphenethylamino)-ethyl]-2(3H)-indolone as the residue. This base in alcohol is treated with an excess of methanesulfonic acid to give the methanesulfonate salt.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04588740 |
| Source dataset | uspto-grants-1986_05 |
| ORD ID | ord-c7c7e9eb37c648118c095d56bb37f520 |
| Source note | uspto-grants-1986_05 |