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Trifluoroacetic acid → 2,2-dimethyl-4-oxo-4H-1,3-benzodioxine-6-carbonitrile

HRID 733508
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반응식

HRID 733508 반응식
[C:1]([C:3]1[CH:11]=[C:7]([C:8]([OH:10])=[O:9])[C:6]([OH:12])=[CH:5][CH:4]=1)#[N:2].[C:13](O)([C:15](F)(F)F)=O.[C:20](OC(C(F)(F)F)=O)(C(F)(F)F)=O>CC(C)=O>[CH3:20][C:13]1([CH3:15])[O:12][C:6]2[CH:5]=[CH:4][C:3]([C:1]#[N:2])=[CH:11][C:7]=2[C:8](=[O:10])[O:9]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 6422Trifluoroacetic acidHCID 9845Trifluoroacetic anhydrideHCID 130269355-Cyano-2-hydroxybenzoic acid

생성물 1

HCID 597024522,2-dimethyl-4-oxo-4H-1,3-benzodioxine-6-carbonitrile수율 18.5%

시약·촉매·용매 1

HCID 180Acetone용매2회

실험 절차

To a suspension of 5-cyano salicylic acid (60 g, 0.368 mol) in TFA (134 mL, 1.76 mol) and TFAA (45 mL, 0.32 mol) was added dry acetone (20 mL) and heated to reflux. After each 1 h interval was added 15 mL of dry acetone for 4 times and the reflux continued for 20 h. The reaction mixture was concentrated under vacuum and crude purified by flash column chromatography over silica gel (230-400 mesh) using CH2Cl2 as an eluent to give the title compound as a white solid (12 g, 15%). TLC: CH2Cl2 (100%), Rf: 0.5

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후처리

  1. temperatureheated to reflux
  2. concentrationThe reaction mixture was concentrated under vacuum and crude
  3. custompurified by flash column chromatography over silica gel (230-400 mesh)

출처 및 근거

ORD 기록
ord-973070df46954464aed7fea6f1334c64
출처 데이터셋
uspto-grants-2009_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07589232B2

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