HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl Acetate → methyl 2-nitro-3-(tetrahydro-2H-pyran-4-yloxy)benzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Oxan-4-yl methanesulfonate | HCID 11344352 | — |
| Reactant | Methyl 3-hydroxy-2-nitrobenzoate | HCID 13659833 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | methyl 2-nitro-3-(tetrahydro-2H-pyran-4-yloxy)benzoate | HCID 58082227 | 136.7% |
Reaction Steps
Methyl 3-hydroxy-2-nitrobenzoate (95 g, 0.52 mol), tetrahydro-2H-pyran-4-yl methanesulfonate (234 g, 1.3 mol) and K2CO3 (358 g, 2.6 mol) was suspend in MeCN (2 L). The mixture was heated at reflux for 20 h. TLC (petroleum ether:ethyl acetate=1:1) showed the reaction was complete. The mixture was filtered; the filtrate was concentrated in vacuo. The residue was purified by chromatography (petroleum ether: ethyl acetate=10:1, 5:1, 2:1) to give the title compound (200 g 100%) as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07998978B2 |
| Source dataset | uspto-grants-2011_08 |
| ORD ID | ord-b87ec786704d44489d96f70a14df63bf |
| Source note | uspto-grants-2011_08 |