HuagongsheHuagongshe Chemistry Print Report · For research reference only
5-(methoxycarbonyl)-1H-indole-2-carboxylic acid → 2-(tert-Butyl)5-methyl1H-indole-2,5-dicarboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 5-(methoxycarbonyl)-1H-indole-2-carboxylic acid | HCID 52987916 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | 1,1-bis(1,1-dimethylethoxy)-N,N,N-trimethylamine | HCID 547712 | — |
| Product | 2-(tert-Butyl)5-methyl1H-indole-2,5-dicarboxylate | HCID 68564796 | — |
Reaction Steps
To 13 g 1H-Indole-2,5-dicarboxylic acid 5-methyl ester in 300 ml toluene, 59 ml Di-tert-butoxymethyl-dimethyl-amine were added dropwise at 80° C. Then, the reaction mixture was heated under reflux for additional 6 h. After removal of the solvents under reduced pressure the residue was dissolved in 300 ml DCM and washed with sat. aqueous NaHCO3 solution (2×100 ml). The organic layer was dried over MgSO4 and concentrated under reduced pressure. The residue was purified by chromatography on silica gel eluting with a n-heptane/ethyl acetate gradient. The fractions containing the product were collected and concentrated under reduced pressure. Yield: 8.3 g. MS (ES+): m/e=276.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07196103B2 |
| Source dataset | uspto-grants-2007_03 |
| ORD ID | ord-bb10148e3fda410994757dc044c9b9a2 |
| Source note | uspto-grants-2007_03 |