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Isobutyric anhydride → Methylene bisisobutyrate

HRID 596981
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HRID 596981 반응식
[O:1]1[CH2:6][CH2:5][CH2:4]OO1.[C:7]([O:12][C:13](=[O:17])[CH:14]([CH3:16])[CH3:15])(=[O:11])C(C)C.Cl(O)(=O)(=O)=O.[C:23](=O)(O)[O-].[Na+]>>[C:13]([O:12][CH2:7][O:11][C:6](=[O:1])[CH:5]([CH3:23])[CH3:4])(=[O:17])[CH:14]([CH3:15])[CH3:16]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 4

HCID 7346Isobutyric anhydrideHCID 24247Perchloric AcidHCID 516892Sodium BicarbonateHCID 19593658CID 19593658

생성물 1

HCID 12851389Methylene bisisobutyrate

실험 절차

A 30-g (0.33 mol) sample of trioxane was added to a solution of 158 g (1 mol) isobutyric anhydride and 0.5 ml 70% perchloric acid over a 30-minute period at 65°-70° C. The reaction mixture was then stirred until the temperature decreased to 27° C. The reaction mixture was diluted with saturated sodium bicarbonate solution and extracted with ether. The ether extracts were dried over magnesium sulfate and evaporated under reduced pressure. The resulting residue was distilled on a 30-cm column to give 112 g of methylene bisisobutyrate, b.p. 43°-48° C. at 0.2-0.3 mm of Hg and 30 g of oxybis-methylene isobutyrate, b.p. 57°-63° C. at 0.2-0.3 mm of Hg.

후처리

  1. customdecreased to 27° C
  2. extractionextracted with ether
  3. dry with materialThe ether extracts were dried over magnesium sulfate
  4. customevaporated under reduced pressure
  5. distillationThe resulting residue was distilled on a 30-cm column

출처 및 근거

ORD 기록
ord-7156f543c297404f9f32044039980fb2
출처 데이터셋
uspto-grants-1977_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04012526

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