HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 74579Generated: October 29, 2026
Hydrochloric Acid → 5-fluoro-3-methyl-2,3-dihydro-1H-indole
https://huagongshe.com/reaction/74579
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Methanol | HCID 887 | — |
| Reactant | Borane | HCID 6331 | — |
| Reactant | 2H-Indol-2-one, 5-fluoro-1,3-dihydro-3-Methyl- | HCID 17792875 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 5-fluoro-3-methyl-2,3-dihydro-1H-indole | HCID 58386694 | — |
Reaction Steps
Under an argon atmosphere 18 mL (18 mmol) of a 1M borane in THF solution was added dropwise to 1.5 g (9.1 mmol) 5-fluoro-3-methyl-1,3-dihydro-indol-2-one in 50 mL THF. The reaction mixture was stirred for 2 h at 70° C., cooled to 0° C. and combined with 10 mL methanol and then with 30 mL semi-concentrated hydrochloric acid solution. The reaction mixture was refluxed for 1 h with stirring, cooled and the organic phase was eliminated using the rotary evaporator. The aqueous phase was extracted with ethyl acetate. The aqueous phase was made alkaline with an aqueous 4M sodium hydroxide solution and extracted with dichloromethane. The organic phase was dried on sodium sulphate, filtered off and evaporated down.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08829006B2 |
|---|
| Source dataset | uspto-grants-2014_09 |
|---|
| ORD ID | ord-075c97acf3964a028a8b4ae314e4ad98 |
|---|
| Source note | uspto-grants-2014_09 |
|---|