Acetic Anhydride → α-(Acetyloxy)-α-methylcyclopropaneacetonitrile

HRID 1766529노트

반응식

HRID 1766529 반응식
[CH:1]1([C:4]([O:8][Si](C)(C)C)([CH3:7])[C:5]#[N:6])[CH2:3][CH2:2]1.[C:13](OC(=O)C)(=[O:15])[CH3:14]>C(#N)C.FC(F)(F)S([O-])(=O)=O.[Sc+3].FC(F)(F)S([O-])(=O)=O.FC(F)(F)S([O-])(=O)=O>[C:13]([O:8][C:4]([CH3:7])([CH:1]1[CH2:3][CH2:2]1)[C:5]#[N:6])(=[O:15])[CH3:14]

참가 물질

5

반응물 2

HCID 7918Acetic AnhydrideHCID 588006alpha-Methyl-alpha-((trimethylsilyl)oxy)cyclopropaneacetonitrile

생성물 1

HCID 21109722α-(Acetyloxy)-α-methylcyclopropaneacetonitrile수율 87.5%

시약·촉매·용매 2

HCID 2734571Scandium(III) triflate촉매HCID 6342Acetonitrile용매

실험 절차

To a well stirred and ice-cooled solution of 2-cyclopropyl-2-trimethylsilanyloxy-propionitrile (188.5 g, 1.03 mol) in acetonitrile (1000 mL) was added acetic anhydride (194 mL, 2.06 mol) and scandium trifluoromethanesulfonate (5 g, 10.3 mmol). The temperature rose to ˜10° C. and stirring was continued for 15′ at room temperature. The solvent was evaporated in vacuo and the residue was distilled to yield 138 g of the title compound as colorless liquid, bp: 84–86° C./6 mbar.

후처리

  1. customrose to ˜10° C.
  2. stirringstirring
  3. customat room temperature
  4. customThe solvent was evaporated in vacuo
  5. distillationthe residue was distilled

출처 및 근거

ORD 기록
ord-e2a29511984045a99ea1651aa472d71d
출처 데이터셋
uspto-grants-2007_06
특허 번호
US07229999B2

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