HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2110345Generated: October 31, 2026
Water → 7-Fluoro-2,3-dihydro-3,3-dimethyl-1H-indole
https://huagongshe.com/reaction/2110345
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 7-fluoro-3,3-dimethyloxindole | HCID 11976436 | — |
| Reactant | Red-Al | HCID 16684438 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 7-Fluoro-2,3-dihydro-3,3-dimethyl-1H-indole | HCID 45142225 | 82% |
Reaction Steps
A mixture of 7-fluoro-3,3-dimethyloxindole (EXAMPLE 99, step 5, 2.24 g 12.5 mmol) in toluene (15 mL) under nitrogen was heated at 80° C. Vitride (65 wt % in toluene, 6 mL, 19.3 mmol) was added dropwise via an addition funnel. The resulting solution was stirred at 80° C. for an additional 1.5 hours, then cooled in an ice bath. Aqueous sodium hydroxide solution (1N, 15 mL) was added slowly to quench the reaction. Water (15 mL) was added and the reaction mixture was extracted with ethyl acetate (20 mL). The organic layer was washed with brine, dried (anhydrous sodium sulfate), filtered through a pad of silica gel, and concentrated under reduced pressure to yield 1.68 g (82%) of 7-fluoro-3,3-dimethylindoline as a colorless oil. MS (ES) m/z 166.1 ([M+H]+); HRMS: calcd for C10H12FN+H+, 166.1032; found (ESI, [M+H]+), 166.1040.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07517899B2 |
|---|
| Source dataset | uspto-grants-2009_04 |
|---|
| ORD ID | ord-6b55913cc8804512b04db2b23517ba18 |
|---|
| Source note | uspto-grants-2009_04 |
|---|