HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzaldehyde → HCID 178473795, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzaldehyde | HCID 240 | — |
| Reactant | Methanol | HCID 887 | — |
| Reactant | HCID 14183251 | HCID 14183251 | — |
| Catalyst | HCID 178418406 | HCID 178418406 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 178473795 | HCID 178473795 | — |
Reaction Steps
A mixture of 2.2 g. (10 mmole) 1-acetyl-5,6-diamino-3,3-dimethylindoline, 200 ml. methanol, 5.2 ml. acetic acid, 1.0 ml. benzaldehyde and 50 mg. manganese dioxide is stirred for 3 hours at ambient temperature while passing in air. The reaction mixture is then filtered, the filtrate evaporated and the residue chromatographed on silica gel. After evaporation of the appropriate fractions and trituration with diethyl ether, there is obtained 0.8 g. (26% of theory) of the title compound; m.p. 225°-227° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04863945 |
| Source dataset | uspto-grants-1989_09 |
| ORD ID | ord-0626c7b84f0048a48d524b7ebf1e5180 |
| Source note | uspto-grants-1989_09 |