HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → HCID 20501032, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Ethanol | HCID 702 | — |
| Reactant | 3-Benzyloxycarbonyl-1-ethoxycarbonyl-1'(3,4-dichlorobenzyl)-spiro[imidazolidine-4,3'-indoline]-2,2',5-trione | HCID 20501034 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Product | HCID 20501032 | HCID 20501032 | 53.5% |
Reaction Steps
A mixture of 3-benzyloxycarbonyl-1-ethoxycarbonyl-1'-(3,4-dichlorobenzyl)spiro[imidazolidine-4,3'-indoline]-2,2',5-trione (1.7 g.), 10% w/w palladium on carbon (0.1 g.), acetic acid (0.3 ml.), ethanol (25 ml.) and 1,2-dimethoxyethane (50 ml.) was hydrogenated at atmospheric pressure for 2 hours. The mixture was separated by filtration through diatomaceous earth and the filtrate was evaporated. The residual oil solidified on treatment with a few drops of toluene. The solid obtained was recrystallised from ethyl acetate/petrol 60-80 to give 1-ethoxycarbonyl-1'-(3,4-dichlorobenzyl)-spiro[imidazolidine-4,3'-indoline]-2,2',5-trione (0.7 g.), 176°-179° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04386100 |
| Source dataset | uspto-grants-1983_05 |
| ORD ID | ord-e78ea9999250417d8e264623f95e726f |
| Source note | uspto-grants-1983_05 |