HuagongsheHuagongshe Chemistry Print Report · For research reference only
Borane → 2-((1S)-6-Bromo-3,4-dihydro-1H-2-benzopyran-1-yl)ethanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Borane | HCID 6331 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 2-((1S)-6-Bromo-3,4-dihydro-1H-2-benzopyran-1-yl)acetic acid | HCID 10635799 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-((1S)-6-Bromo-3,4-dihydro-1H-2-benzopyran-1-yl)ethanol | HCID 53687843 | — |
Reaction Steps
To a solution of 2-((1S)-6-bromo-3,4-dihydro-1H-2-benzopyran-1-yl)acetic acid (21.3 g, 78.6 mmol) in anhydrous THF (65 mL) under an atmosphere of nitrogen and cooled to 0° C., was added dropwise borane.THF complex in THF (1M) (94 mL, 94 mmol). After stirring for 1 h between 0 and 10° C., the reaction mixture was treated with aqueous sodium carbonate then extracted into toluene. The organic layer was washed with dilute aqueous hydrochloric acid, then concentrated in vacuo to give the title compound as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07335660B2 |
| Source dataset | uspto-grants-2008_02 |
| ORD ID | ord-c2052c3b95db415d840ea13208e9a876 |
| Source note | uspto-grants-2008_02 |