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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 127441Generated: October 29, 2026

Nitric Acid → 6-Nitro-8-acetamino-1,4-benzodioxane-5-carboxylic acid

https://huagongshe.com/reaction/127441

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitric AcidHCID 944—
ReactantAcetic AnhydrideHCID 7918—
Reactant8-Acetamido-1,4-benzodioxan-5-carboxylic acidHCID 14956207—
SolventAcetic AcidHCID 176—
Product6-Nitro-8-acetamino-1,4-benzodioxane-5-carboxylic acidHCID 20544717—
Product7-Nitro-8-acetamino-1,4-benzodioxane-5-carboxylic acidHCID 20544747—

Reaction Conditions

Temperature20 °C

Reaction Steps

42 g of 8-acetamino-1,4-benzodioxane-5-carboxylic acid, 75 ml of acetic acid and 75 ml of acetic anhydride were introduced into a balloon flask and then a solution of 17.5 ml of nitric acid (d=1.49) in 17 ml of acetic acid was added, with the temperature being left rising. After dissolution and crystallization, 50 ml of acetic acid were added. The mixture was agitated at 40°-45° C. and then cooled to 20° C. The precipitate was dried off, washed with acetic acid and water and dried. 13.5 g of a 50% mixture of 7-nitro-8-acetamino-1,4-benzodioxane-5-carboxylic acid and 6-nitro-8-acetamino-1,4-benzodioxane-5-carboxylic acid were obtained. The 7-nitro-8-acetamino-1,4-benzodioxane-5-carboxylic acid was separated and then treated according to the process of Example 31 with isobutyl chloroformate and diethylaminoethylamine. N-(diethylaminoethyl)-7-nitro-8-acetamino-1,4-benzodioxane-5-carboxamide was obtained. The structure was confirmed by nuclear magnetic resonance analysis.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04255580
Source datasetuspto-grants-1981_03
ORD IDord-5e029a19e76b4cf99f3a2cdb701f6c4c
Source noteuspto-grants-1981_03