HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 127442Generated: October 25, 2026
Nitric Acid → 6-Nitro-2,3-dihydro-1,4-benzodioxine-5-carboxylic acid
https://huagongshe.com/reaction/127442
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Nitric Acid | HCID 944 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | 2,3-Dihydro-1,4-benzodioxin-5-carboxylic acid | HCID 78184 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 6-Nitro-2,3-dihydro-1,4-benzodioxine-5-carboxylic acid | HCID 12464531 | — |
Reaction Steps
1,600 ml of acetic acid, 1,600 ml of acetic anhydride, and 1000 g of 1,4-benzodioxane-5-carboxylic acid were introduced in a 6-liter balloon flask provided with an agitator and a thermometer. The mixture was heated to 40° C. and a solution of 400 ml of nitric acid in 400 ml of acetic acid was added. After the introduction, the mixture was stirred at 40°-45° C. for two hours and then cooled to 5° C. The precipitate was dried off, washed with 600 ml of acetic acid and then with water and dried at 40° C. 700 g of 7-nitro-1,4-benzodioxane-5-carboxylic acid were collected, the structure of which was confirmed by nuclear magnetic resonance (M.P.: 246° C.) The mother liquors were diluted with 25 liters of water and the obtained precipitate was dried off, washed with water and dried. 6-nitro-1,4-benzodioxane-5-carboxylic acid was obtained (M.P.: 188° C.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04255580 |
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| Source dataset | uspto-grants-1981_03 |
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| ORD ID | ord-2eaf11dd36b849af9e7225cfd14c5631 |
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| Source note | uspto-grants-1981_03 |
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