HuagongsheHuagongshe Chemistry Print Report · For research reference only
tert-Butanol → 2-(2-Chlorophenylamino)-3,4-difluoro-6-formylbenzoic acid methyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | tert-Butanol | HCID 6386 | — |
| Reactant | Methyl morpholine oxide | HCID 82029 | — |
| Reactant | Sodium periodate | HCID 23667635 | — |
| Reactant | 2-(2-Chlorophenylamino)-3,4-difluoro-6-styrylbenzoic acid methyl ester | HCID 86598595 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | Oxolane--water (1/1) | HCID 21881883 | — |
| Product | 2-(2-Chlorophenylamino)-3,4-difluoro-6-formylbenzoic acid methyl ester | HCID 86598596 | 755.5% |
Reaction Steps
A mixture of 2-(2-chlorophenylamino)-3,4-difluoro-6-styrylbenzoic acid methyl ester (1.20 g, 3.00 mmol), 2.5% OSO4 solution in t-BuOH (2.0 mL, 0.165 mmol) and NMO (0.435 g, 3.60 mmol) in 30 mL of 1:1 THF/water was stirred for 1 hour. Sodium periodate (0.963 g, 4.50 mmol) was added. After 1 hour, the reaction mixture was diluted with ethyl acetate and water and the layers separated. The organic layer was dried (MgSO4) and concentrated under reduced pressure. Purification by flash column chromatography (1:1 methylene chloride/hexanes) gave 0.406 g (42%) pure desired product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07485643B2 |
| Source dataset | uspto-grants-2009_02 |
| ORD ID | ord-1bbd2f881432432ba73b368f5f87016c |
| Source note | uspto-grants-2009_02 |