HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → (1-methyl-1H-indol-2-yl)methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | methyl 1-methyl-1H-indole-2-carboxylate | HCID 258548 | — |
| Reactant | Lithium borohydride | HCID 4148881 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (1-methyl-1H-indol-2-yl)methanol | HCID 295652 | 99.9% |
Reaction Steps
A solution of 5.05 g of methyl 1-methylindole-2-carboxylate (prepared as described in Preparation 22) in 20 ml of anhydrous tetrahydrofuran was added dropwise to a mixture of 1.85 g of lithium borohydride and 80 ml of anhydrous tetrahydrofuran, and the resulting mixture was heated under reflux for 4 hours. At the end of this time, the reaction mixture was poured into water, after which it was extracted with ethyl acetate. The extract was washed with an aqueous solution of sodium chloride and dried over anhydrous sodium sulfate. The solvent was then removed by distillation under reduced pressure, to give 4.30 g of the title compound, melting at 92.8°-95.2° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05834501 |
| Source dataset | uspto-grants-1998_11 |
| ORD ID | ord-e511a4ad8d7e402fb0798aafb3d64739 |
| Source note | uspto-grants-1998_11 |