HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → [2-(Trifluoromethyl)-1H-indol-3-yl]methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Potassium borohydride | HCID 4192641 | — |
| Reactant | 2-trifluoromethyl-3-formyl-(1H)-indole | HCID 20032128 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | [2-(Trifluoromethyl)-1H-indol-3-yl]methanol | HCID 20032113 | 64.6% |
Reaction Steps
2 g of potassium borohydride were added in small fractions at +5° C. to a solution of 4.6 g of the product of Step A, 150 ml of tetrahydrofuran and 30 ml of water and the mixture was stirred for one hour. The mixture was allowed to return to ambient temperature and the tetrahydrofuran was eliminated under reduced pressure. The resulting mixture was diluted with ether, washed with water, dried and concentrated under reduced pressure. The residue was chromatographed over silica (eluent: hexaneethyl acetate 7-3) to obtain 3 g of 2-trifluoromethyl-(1H)-indol-3-yl methanol melting at 106° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04849443 |
| Source dataset | uspto-grants-1989_07 |
| ORD ID | ord-ad967951fb5a48f7bfe9f3319054f3fa |
| Source note | uspto-grants-1989_07 |