HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 488534Generated: October 26, 2026
Dimethylformamide → 5-Bromo-1-methyl-1H-indole
https://huagongshe.com/reaction/488534
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Dabco | HCID 9237 | — |
| Reactant | 5-Bromoindole | HCID 24905 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 5-Bromo-1-methyl-1H-indole | HCID 285757 | 989.4% |
Reaction Steps
To a solution of 5-bromoindole (1.0 g, 5.10 mmol) in DMC (10 mL), DABCO (0.057 g, 0.51 mmol) is added followed by DMF (1 mL). The resulting solution is heated to 90-95° C. for 5 h. The reaction is cooled to RT, and diluted with ethyl acetate (EtOAc, 50 mL) and H2O (50 mL). The organic layer is separated and washed in sequence with H2O (50 mL), 10% aqueous citric acid (2×50 mL) and H2O (4×50 mL). The organic layer is dried over anhydrous sodium sulfate (Na2SO4), filtered and concentrated under vacuum to give 5-bromo-1-methylindole (about 1.06 g, 99%) as a golden colored solid: 1H NMR (CDCl3) δ7.72 (d, 1H), 7.26 (dd, 1H), 7.13 (d, 1H), 7.00 (d, 1H), 6.39 (d, 1H), 3.71 (s, 3H); 13C NMR (CDCl3) δ135.3, 130.1, 129.9, 124.2, 123.2, 112.6, 110.6, 100.5, 32.9; MS m/z 209 [M+1]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06972336B2 |
|---|
| Source dataset | uspto-grants-2005_12 |
|---|
| ORD ID | ord-fcd99546cab64b19be0a13349eb9b61d |
|---|
| Source note | uspto-grants-2005_12 |
|---|