HuagongsheHuagongshe Chemistry Print Report · For research reference only
Isopropanol → Isopropyl 3-methyl-1h-indole-2-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Isopropanol | HCID 3776 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | ethyl 3-formyl-1H-indole-2-carboxylate | HCID 5107764 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Product | Isopropyl 3-methyl-1h-indole-2-carboxylate | HCID 22311011 | 25% |
Reaction Steps
Sodium borohydride (0.23 g) was added to a stirred solution of ethyl 3-formylindole-2-carboxylate (0.2 g) and 10% palladium on carbon (0.11 g) in isopropanol (45 ml). The solution was heated at reflux for 4 hours, cooled and filtered through Celite. The solution was partitioned between ethyl acetate and water. Combined organic extracts were dried (MgSO4) and concentrated in vacuo and the residue purified by column chromatography using isohexane-10% ethyl acetate as eluent to give the desired end product as a white solid (0.05 g, 25%); NMR δ(CD3SOCD3) 1.3 (d, 6H), 2.5 (s, 3H), 5.2 (m, 1H), 7.0 (m, 1H), 7.2 (m, 1H), 7.4 (m, 1H), 7.6 (d, 1H), 11.3 (bs, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06441004B1 |
| Source dataset | uspto-grants-2002_08 |
| ORD ID | ord-971703a055824de9b6518988027451b4 |
| Source note | uspto-grants-2002_08 |