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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2083122Generated: November 2, 2026

Sulfuric Acid → HCID 20135952, compound

https://huagongshe.com/reaction/2083122

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
ReactantSulfur trioxideHCID 24682—
ReactantPerfluoro(N-methylmorpholine)HCID 67839—
ReactantHCID 20359822HCID 20359822—
ProductHCID 20135952HCID 20135952—

Reaction Conditions

Temperature25 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04084050
Source datasetuspto-grants-1978_04
ORD IDord-03ade2d2fb9449298dc0d305f78ccb4a
Source noteuspto-grants-1978_04