HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-bromobutanimide → 1-Tert-butyl 7-methyl 5-bromoindoline-1,7-dicarboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 1-Tert-butyl 7-methyl indoline-1,7-dicarboxylate | HCID 49758857 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-Tert-butyl 7-methyl 5-bromoindoline-1,7-dicarboxylate | HCID 49758856 | 89% |
Reaction Steps
1-(1,1-dimethylethyl) 7-methyl 2,3-dihydro-1H-indole-1,7-dicarboxylate (3.1 g, 11.2 mmol) and N-bromosuccinimide (2.0 g, 11.2 mmol) were dissolved in dry dichloromethane (100 mL) and stirred under a nitrogen atmosphere at room temperature for 16 hours. The reaction was partitioned with sodium hydroxide solution (2 M), separated and washed with more sodium hydroxide solution. The organic layer was dried over magnesium sulfate and concentrated in vacuo to give the title compound as a gummy red solid (3.55 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08063071B2 |
| Source dataset | uspto-grants-2011_11 |
| ORD ID | ord-630d134d786c4515b9e3e7eb258db42f |
| Source note | uspto-grants-2011_11 |