Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | HCID 18391224 | HCID 18391224 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 68507957 | HCID 68507957 | 99.2% |
Reaction Steps
(S)-5-Bromo-indan-2-carboxylic acid (12.65 mmol) was dissolved in dry THF (75 mL). The mixture was cooled with stirring to 0-2° C. under argon. 1M BH3 in THF (18.4 mL; 18.4 mmol) was added via syringe at a rapid dropwise rate. The mixture was stirred at 0° C. for 30 minutes then allowed to warm to rt and stir for 90 minutes. The reaction mixture was cooled again to 0° C. and treated carefully with 10 mL of water. Volatiles were removed under reduced pressure and the residue partitioned between diethyl ether (100 mL) and brine (50 mL). The aqueous phase was extracted with 100 mL ethyl ether and each extract washed with brine. The combined extracts were dried over Na2SO4, filtered and volatiles were removed under reduced pressure to give 2.85 g of ((S)-5-bromo-indan-2-yl)-methanol as a crystalline white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07803816B2 |
|---|
| Source dataset | uspto-grants-2010_09 |
|---|
| ORD ID | ord-0d1cd795e892459293430bf41c6d1d56 |
|---|
| Source note | uspto-grants-2010_09 |
|---|