HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 82340Generated: October 25, 2026
Phthalic Anhydride → 2-(3-(Tert-butoxycarbonyl)phenyl)-3-methylpyridine 1-oxide
https://huagongshe.com/reaction/82340
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phthalic Anhydride | HCID 6811 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Sodium Sulfite | HCID 24437 | — |
| Reactant | Carbamide Peroxide | HCID 31294 | — |
| Reactant | tert-Butyl 3-(3-methylpyridin-2-yl)benzoate | HCID 57516851 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 2-(3-(Tert-butoxycarbonyl)phenyl)-3-methylpyridine 1-oxide | HCID 58488371 | 95% |
Reaction Steps
tert-Butyl-3-(3-methylpyridin-2-yl)benzoate (1.0 eq) is dissolved in EtOAc (6 vol). Water (0.3 vol) is added followed by urea-hydrogen peroxide (3 eq). The phthalic anhydride (3 eq) is added portion-wise as a solid to maintain the temperature in the reactor below 45° C. After completion of phthalic anhydride addition, the mixture is heated to 45° C. After stirring for an additional 4 hours, the heat is turned off 10% w/w aqueous Na2SO3 (1.5 eq) is added via addition funnel. After completion of Na2SO3 addition, the mixture is stirred for an additional 30 minutes and the layers separated. The organic layer is stirred and 10% w/w aq. Na2CO3 (2 eq) is added. After stirring for 30 minutes, the layers are allowed to separate. The organic phase is washed 13% w/v aq NaCl. The organic phase is then filtered and concentrated to afford crude 2-(3-(tert-butoxycarbonyl)phenyl)-3-methylpyridine-1-oxide (95%) that is used directly in the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08846718B2 |
|---|
| Source dataset | uspto-grants-2014_09 |
|---|
| ORD ID | ord-4be228e010c64484b8d943db955dd51f |
|---|
| Source note | uspto-grants-2014_09 |
|---|