HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → 2-Chloro-1-(6-fluoro-1-benzopyran-2-yl)-ethanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 2-Chloro-1-(6-fluoro-1-benzopyran-2-yl)-ethanone | HCID 86657994 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-Chloro-1-(6-fluoro-1-benzopyran-2-yl)-ethanol | HCID 67212507 | 70% |
Reaction Steps
A stirred solution of 2-Chloro-1-(6-fluoro-1-benzopyran-2-yl)-ethanone (0.33 g, 1.28 mmol, 88.4% A) in ethanol (2.5 ml) was cooled to 0° C. under nitrogen. NaBH4 (60.1 mg, 1.59 mmol) was added to the solution and the reaction mixture stirred for 2 hours. After checking by GPC that the starting product had disappeared, the mixture was diluted with demineralized water (7 ml) and dichloromethane (7 ml) and the phases separated. The organic layer was dried over anhydrous sodium sulphate, filtered and concentrated under vacuum to give crude 2-Chloro-1-(6-fluoro-1-benzopyran-2-yl)-ethanol as a mixture of diastereoisomers 54:46 (0.30 g, 70% yield, 67.9% A).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08981127B2 |
| Source dataset | uspto-grants-2015_03 |
| ORD ID | ord-be09a0a66b9d45849aaa9811caf8eb00 |
| Source note | uspto-grants-2015_03 |