HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2215789Generated: November 3, 2026
Methyl iodide → 7-Bromo-5-fluoro-1-methyl-1H-indole
https://huagongshe.com/reaction/2215789
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 7-bromo-5-fluoro-1H-indole | HCID 3852879 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 7-Bromo-5-fluoro-1-methyl-1H-indole | HCID 21950063 | — |
Reaction Steps
To a suspension of sodium hydride (60%, 1.75 g, 43.8 mmol) in DMF (134 mL) was added a solution of 5-fluoro-7-bromoindole (7.8 g, 36.4 mmol) in DMF (10 mL). After 1 h at room temperature, the mixture was treated with methyl iodide (3.4 mL, 54.6 mmol) with cooling in an ice-water bath. The reaction mixture was allowed to warm up room temperature and stirred overnight. The reaction was quenched with water, extracted with ethyl acetate, and the organic layer was washed with water and brine, dried (sodium sulfate) and concentrated to give a crude product, which was used without further purification. 1H NMR (400 MHz, CDCl3) 4.06 (s, 3H), 6.34 (d, J=3.13 Hz, 1H), 6.96 (d, J=3.13 Hz, 1H), 7.07 (dd, J1=2.34 Hz, J2=8.60 Hz, 1H), 7.12 (dd, J1=2.34 Hz, J2=9.0 Hz, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07109229B2 |
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| Source dataset | uspto-grants-2006_09 |
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| ORD ID | ord-f968cbe16e6748b1bc6bcf5d7126b312 |
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| Source note | uspto-grants-2006_09 |
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