Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Sulfur trioxide | HCID 24682 | — |
| Reactant | Perfluoro(N-methylmorpholine) | HCID 67839 | — |
| Reactant | HCID 20359822 | HCID 20359822 | — |
| Product | HCID 20135952 | HCID 20135952 | — |
Reaction Steps
To 253 g. (0.85 mol) of perfluoro-(N-methyl-morpholine) in a 300 ml. autoclave is added 72 g. (0.9 mol) of sulfur trioxide. The vessel is sealed, heated and rocked at 120° C. for 6 hrs. The autoclave is then cooled to 25° C., vented to release volatile materials and the residue charged to a 500 cc. flask equipped with magnetic stirrer, dropping funnel, condenser and thermometer. A solution of 195 g. of 96% sulfuric acid and 5 g. of H2C is added dropwise with stirring. The temperature is kept below 50° C. After the sulfuric acid is added the mixture is heated and stirred at reflux (55°-60° C.) for four hours. Distillation yields a large fraction, 207 g., b.p. 48°-65° C./740 mm., which consists of 45% by weight perfluoror-N-methyl-3-oxo-morpholine (40% conversion) and 15% by weight of higher boiling products believed to include perfluoro-(N-methyl-3,5dioxo-morpholine). Isolation of the pure amide (b.p. 59°-60° C./740 mm.) can be accomplished by distillation through a 25-plate column.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04084050 |
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| Source dataset | uspto-grants-1978_04 |
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| ORD ID | ord-03ade2d2fb9449298dc0d305f78ccb4a |
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| Source note | uspto-grants-1978_04 |
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