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HRID 129354생성일: 2026년 10월 25일

Acrylic Acid → N-[3-(Dimethylamino)propyl]-N-[(nonafluorobutyl)sulfonyl]-beta-alanine

https://huagongshe.com/reaction/129354

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참여 물질

역할이름HCID투입량
반응물Acrylic AcidHCID 6581—
반응물PhenothiazineHCID 7108—
반응물Diethylene Glycol Monobutyl EtherHCID 8177—
반응물1-Butanesulfonamide, N-[3-(dimethylamino)propyl]-1,1,2,2,3,3,4,4,4-nonafluoro-HCID 110558—
용매WaterHCID 962—
생성물N-[3-(Dimethylamino)propyl]-N-[(nonafluorobutyl)sulfonyl]-beta-alanineHCID 15251601—

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온도125 °C

반응 단계

An acrylic acid Michael addition reaction was then run according to the general procedure given in U.S. Pat. No. 5,144,069 (Stern et al.). 50 g (0.12 mole) of the purified C4F9SO2N(H)C3H6N(CH3)2, 16.4 g (0.23 mole) of acrylic acid and 0.2 g of phenothiazine (free radical polymerization inhibitor) were added to a 250-mL three-neck flask equipped with an air stirrer and thermometer. The resulting mixture was heated to 125° C. and was allowed to react for 6 hours. After this reaction period, a positive solubility check of the product in water of pH 7 indicated that the Michael addition reaction was essentially complete. While still mixing, a solvent blend of 18 g of diethylene glycol monobutyl ether and 42 g of deionized water was added and the mixture was allowed to cool to room temperature. The water solubility test was run again with the same positive result, showing good conversion to the desired Michael addition product, C4F9SO2N(C2H4COOH)C3H6 (CH3)2.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05468353
출처 데이터셋uspto-grants-1995_11
ORD IDord-6db07f2762984316b90d6f5c14a17a70
출처 메모uspto-grants-1995_11