HuagongsheHuagongshe Chemistry Print Report · For research reference only
Indoline-2-carboxylic acid, (S)- → (S)-(+)-2-Indolinemethanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Indoline-2-carboxylic acid, (S)- | HCID 2733920 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (S)-(+)-2-Indolinemethanol | HCID 6951186 | 87% |
Reaction Steps
To a solution of (S)-indoline-2-carboxylic acid (9.2 mmol, 1.0 equiv.) in THF (18 ml) was added dropwise BH3-DMS solution (18.4 mmol, 2 equiv.) and the reaction mixture was heated to reflux for 12 h. The mixture was quenched with methanol (7.5 ml) and conc. HCl (2.5 ml) with cooling and was then refluxed for additional 2 h. The solvent was evaporated and the residue was basified with 40% NaOH solution and extracted with dichloromethane. The organic layer was washed with brine, dried over sodium sulfate and the solvent was evaporated under reduced pressure to give the crude product which was purified by silica gel column chromatography. Yield: 87%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08541573B2 |
| Source dataset | uspto-grants-2013_09 |
| ORD ID | ord-5980e20ebdce4253b889a339eb09cf2f |
| Source note | uspto-grants-2013_09 |