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Nitric Acid → 3H-1,2-benzodioxole

HRID 248807
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HRID 248807 반응식
C[C:2]1([C:11]2[CH:16]=[CH:15][C:14](C(F)(F)F)=[CH:13][CH:12]=2)OC2C=CC=CC=2[O:3]1.[N+]([O-])(O)=[O:22].O>ClC(Cl)C>[O:22]1[C:12]2[CH:13]=[CH:14][CH:15]=[CH:16][C:11]=2[CH2:2][O:3]1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 944Nitric AcidHCID 962WaterHCID 189611982-Methyl-2-[4-(trifluoromethyl)phenyl]-1,3-benzodioxole

생성물 1

HCID 167221333H-1,2-benzodioxole수율 82%

시약·촉매·용매 1

HCID 63651,1-Dichloroethane용매

반응 조건

온도
20 °C

실험 절차

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

A solution of 2-methyl-2-[4-(trifluoromethyl)phenyl]-1,3-benzodioxole (5.6g) in dichloroethane (15 ml) was added over 10 minutes to vigorously stirred nitric acid (50% w/v, 25 ml) keeping the temperature at 15°-20° C. by means of a cooling bath. The resulting reaction mixture was stirred for a further 1 hour at 20° C., poured into water (200 ml) and extracted with methylene chloride (3×100 ml). After drying over anhydrous sodium sulphate, the extract was evaporated under reduced pressure. The residue was purified by chromatography on silica gel using methylene chloride as eluant, affording the pure product benzodioxole as a pale yellow oil (5.3 g, 82%).

후처리

  1. customat 15°-20° C.
  2. customThe resulting reaction mixture
  3. extractionextracted with methylene chloride (3×100 ml)
  4. dry with materialAfter drying over anhydrous sodium sulphate
  5. customthe extract was evaporated under reduced pressure
  6. customThe residue was purified by chromatography on silica gel

출처 및 근거

ORD 기록
ord-2b7ac7210934401daa920094597419d4
출처 데이터셋
uspto-grants-1993_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05212171

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