HuagongsheHuagongshe Chemistry Print Report · For research reference only
Nitric Acid → 5-Nitro-2-(2,2,2-trifluoroethyl)-2-trifluoromethyl-1,3-benzodioxole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Nitric Acid | HCID 944 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | 2-(2,2,2-Trifluoroethyl)-2-(trifluoromethyl)-1,3-benzodioxole | HCID 53667303 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 5-Nitro-2-(2,2,2-trifluoroethyl)-2-trifluoromethyl-1,3-benzodioxole | HCID 53877230 | — |
Reaction Steps
A solution of 54.4 g of 2-(2,2,2-trifluoroethyl)-2-trifluoromethyl-1,3-benzodioxole in 75 ml of methylene chloride was added dropwise at 10° C. to a mixture of 40 ml of 65% strength by weight nitric acid and 40 ml of concentrated sulphuric acid. Stirring was continued for 1 hour at room temperature and the batch was then poured into ice-water, the organic phase was separated off, and the aqueous phase was extracted using methylene chloride. The combined organic phases were washed with water, dried and freed from volatile components. 95 g of the product (=86% of theory), which had a melting point of 87° to 88° C., remained. The NMR spectra showed the following characteristic absorptions: 19F-NMR: -59.0 and -69.4 ppm. 1H-NMR: 3.10 ppm.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05863933 |
| Source dataset | uspto-grants-1999_01 |
| ORD ID | ord-ae0adfc5fd8f4d49b07e6aa955b71d90 |
| Source note | uspto-grants-1999_01 |