HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 725246Generated: October 30, 2026
Sodium Hydroxide → 2,2,7-Trimethyl-1,3-dioxolo-[4,5-g]-quinoxaline-6-carboxylic acid, 1,1-dimethylethyl ester
https://huagongshe.com/reaction/725246
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Tetrafluoro-m-phenylenediamine dihydrochloride | HCID 149026 | — |
| Reactant | Tert-butyl 2,3-dioxobutanoate | HCID 10986731 | — |
| Reactant | HCID 13343758 | HCID 13343758 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2,2,7-Trimethyl-1,3-dioxolo-[4,5-g]-quinoxaline-6-carboxylic acid, 1,1-dimethylethyl ester | HCID 54007473 | — |
Reaction Steps
[5,6-diamino-2,2-dimethyl-1,3-benzodioxole; dihydrochloride salt] (U.S. Pat. No. 4,904,775, Example 3D) (6.8 g, 0.02 mmol) was dissolved in a mixture of 25 ml water and 10 ml tetrahydrofuran and the pH of the solution was adjusted to 5.5 by the addition of 2N NaOH. After addition of the compound from Example 1 (3.8 g; 0.02 mol) the mixture was refluxed for 2 hours, concentrated in vacuo to remove the organic solvent tetrahydrofuran and then extracted with ethyl acetate. The combined organic phases were washed with brine, dried (Na2SO4) and then evaporated in vacuo to leave an oil which crystallized by the addition of petroleum ether. M.P. 104°-105° C.; yield 5.2 g (82%). C17H20N2O4 % C calc. 64.54%, found 64.40% % H calc. 6.37%, found 6.41% % N calc. 8.85%, found 8.86%
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05705645 |
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| Source dataset | uspto-grants-1998_01 |
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| ORD ID | ord-699b74c1d37f48d3956f8cfc88094db9 |
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| Source note | uspto-grants-1998_01 |
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