HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 5-(trifluoromethyl)-2,3-dihydro-1H-indole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 5-(trifluoromethyl)-1H-indole | HCID 2763075 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 5-(trifluoromethyl)-2,3-dihydro-1H-indole | HCID 15447789 | 45% |
Reaction Steps
5-Trifluoromethylindole (D5, 1.0 g, 0.0057 mole) in glacial acetic acid (25 ml) was treated with sodium cyanoborohydride (1.7 g, 0.027 mole) under argon and stirred at room temperature for 2 hours. The mixture was poured into water (200 ml), basified with 40% aqueous sodium hydroxide solution, extracted into DCM, dried (Na2SO4) and evaporated in vacuo. The residue was chromatographed on silica gel eluting with 20% ethyl acetate/60-80° petroleum ether to afford the title compound (0.45 g, 45%) as a pale yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06313145B1 |
| Source dataset | uspto-grants-2001_11 |
| ORD ID | ord-f8d37cd7232d431c9a830344053fb51a |
| Source note | uspto-grants-2001_11 |