HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2253553Generated: October 26, 2026
Nitric Acid → 1,2-Dichloro-1,2-difluoro-1-nitroethyl trifluoroacetate
https://huagongshe.com/reaction/2253553
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Nitric Acid | HCID 944 | — |
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Dichlorodifluoroethene | HCID 11736 | — |
| Reactant | Chlorofluoronitroacetic Acid | HCID 13452256 | — |
| Reactant | Oleum Trifluoroacetic Acid | HCID 131718034 | — |
| Solvent | Fuming sulfuric acid | HCID 24681 | — |
| Product | 1,2-Dichloro-1,2-difluoro-1-nitroethyl trifluoroacetate | HCID 53881149 | 14.5% |
Reaction Steps
Chlorofluoronitroacetic Acid, Oleum-Trifluoroacetic Acid Procedure. A solution of 100% nitric acid (5 mL) and trifluoroacetic acid (4.2 mL, 54 mmol) in 30% oleum (6 mL) was added over 25 min to 1,2-dichlorodifluoroethylene (7.5 g, 56 mmol) at 10°-15° C. The mixture was stirred for 60 min at 10°-14° C. The organic layer was separated, and fractionally distilled to give 2.1 g (14.5%) of 1,2-dichloro-1,2-difluoro-1-nitroethyl trifluoroacetate, as a 50:50 mixture of diasterimers, bp 48°-50° C. (0.5 mm): 19F NMR (CDCl3 ) δ -76.27 (s, 6 F), -77.50 (s,1 F), -78.49 (s, 1F), -94.37 (s, 1 F), -95.30 (s, 1 F). The second fraction contained 4.0 g of chlorofluoronitroacetic acid, bp 55°-65° C. (0.5 mm), identical to the authentic material prepared above. The oleum layer was heated to 80° C. under vacuum (0.5 mm) to give an additional 1.61 g (63% combined yield) of chlorofluoronitroacetic acid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | USH0001223 |
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| Source dataset | uspto-grants-1993_08 |
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| ORD ID | ord-ebbc716f35704f0699fb2853a54618dd |
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| Source note | uspto-grants-1993_08 |
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