Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 22890221 | HCID 22890221 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 298221-40-6 | HCID 23446878 | — |
Reaction Steps
At 22° C., 110 g (0.52 mol of 6-chloro-3-methylisatoic anhydride were introduced into a mixture of 750 ml of methanol and 47.6 g (0.47 mol) of triethylamine, and the mixture was then stirred at 65° C. for 2 h. The reaction mixture was concentrated under reduced pressure and the residue was taken up in methylene chloride and extracted 3 times with 0.5 N aqueous sodium hydroxide solution. The mixture was dried over magnesium sulfate, filtered through silica gel and concentrated under reduced pressure, giving 45.5 g (43.8% of theory) of the title compound as a colorless oil with nD23=1.5765.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06472349B1 |
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| Source dataset | uspto-grants-2002_10 |
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| ORD ID | ord-da7b1bdb405e49098cc78eceaa7e2eae |
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| Source note | uspto-grants-2002_10 |
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