HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → 2,2-Difluoro-2-phenylethanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | Ethyl 2,2-difluoro-2-phenylacetate | HCID 10631860 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2,2-Difluoro-2-phenylethanol | HCID 9793891 | 97.8% |
Reaction Steps
A stirred mixture of 2.2 g of difluoro-2-phenyl acetic acid ethyl ester (W. J. Middleton, E. M. Bingham, J. Org. Chem., 45, 2883-2887 (1980)), and 0.6 g of sodium borohydride in 75 mL of ethanol was kept at room temperature overnight, concentrated to near dryness under reduced pressure carefully acidified with 20 mL of 5% HCl and extracted into 3×50 mL of dichloromethane. The combined extracts were dried over magnesium sulfate and concentrated under reduced pressure. Drying under vacuum gave 1.7 g of product as an oil: 1H NMR (400 MHz, CDCl3) 7.5 (m, 5H), 4.0 (t, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07452893B2 |
| Source dataset | uspto-grants-2008_11 |
| ORD ID | ord-9e6fbc5b68eb4c49afe95970aca491c6 |
| Source note | uspto-grants-2008_11 |