HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → 1-Acetyl-5-carbomethoxy-7-chloro-4-methoxy-1,2-dihydroindole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | 1-Acetyl-5-carbomethoxy-7-chloro-4-methoxyindole | HCID 10493103 | — |
| Catalyst | Platinum | HCID 23939 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 1-Acetyl-5-carbomethoxy-7-chloro-4-methoxy-1,2-dihydroindole | HCID 10564950 | — |
Reaction Steps
The mixture of the indole of step 8 above (0.9 g) and Pt-C (0.2 g), acetic acid and MeOH (100 ml) is stirred under H2 at 1 atm. pressure for 48 hours. The catalyst is filtered (celite), the filtered material is washed (MeOH) and the reaction mixture and methanol washings are evaporated. The residue is diluted with CH2Cl2, washed with saturated NaHCO3, dried (MgSO4) and evaporated affording a colorless, semicrystalline material which is determined to be the desired compound by NMR. M.P. 107°-109° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04920219 |
| Source dataset | uspto-grants-1990_04 |
| ORD ID | ord-be1d126f7a2a4da2bef77007ed389b1e |
| Source note | uspto-grants-1990_04 |