HuagongsheHuagongshe Chemistry Print Report · For research reference only
m-Chloroperbenzoic acid → 4'-Fluoro-3-(1-methylethyl)[1,1'-biphenyl]-2-ol formate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | 4'-Fluoro-3-(1-methylethyl)[1,1'-biphenyl]-2-carboxaldehyde | HCID 19004465 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4'-Fluoro-3-(1-methylethyl)[1,1'-biphenyl]-2-ol formate | HCID 19004388 | 66.1% |
Reaction Steps
3-Chloroperbenzoic acid (4.73 g) was added to a solution of 4'-fluoro-3-(1-methylethyl)[1,1'-biphenyl]-2-carboxaldehyde (3.55 g) in dichloromethane (100 mL) and the reaction mixture was stirred at room temperature overnight. The precipitated solids were removed by filtration and the filtrate was washed in turn with water, saturated sodium bisulfite solution, sodium bicarbonate solution and brine. After the dried (MgSO4) organic layer was evaporated, the crude product was purified by HPLC (ethyl acetate-hexane; 1:49) to afford 2.5 g of 4'-fluoro-3-(1-methylethyl)[1,1'biphenyl]-2-ol formate as a oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05344843 |
| Source dataset | uspto-grants-1994_09 |
| ORD ID | ord-4f5c1c27fdd84077a1a5a2d9f8e4387f |
| Source note | uspto-grants-1994_09 |