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Acetone → HCID 23077311, 화합물

HRID 1350608
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HRID 1350608 반응식
[CH3:1][C:2](C)=O.[F:5][C:6]1[C:15]2[C:10](=[CH:11][CH:12]=[C:13]([F:17])[C:14]=2[F:16])[CH:9]=[CH:8][C:7]=1[OH:18].C(=O)([O-])[O-].[K+].[K+].C(I)C>C1(C)C=CC=CC=1>[CH2:1]([O:18][C:7]1[CH:8]=[CH:9][C:10]2[C:15](=[C:14]([F:16])[C:13]([F:17])=[CH:12][CH:11]=2)[C:6]=1[F:5])[CH3:2]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 180AcetoneHCID 6340IodoethaneHCID 11430Potassium CarbonateHCID 230773061,7,8-Trifluoronaphthalen-2-ol

생성물 1

HCID 23077311HCID 23077311, 화합물

시약·촉매·용매 1

HCID 1140Toluene용매

실험 절차

An acetone (80 ml) solution of 1,7,8-trifluoro-2-naphthol (15 g), potassium carbonate (16 g), and ethyl iodide (26 g) was stirred for 10 hours at room temperature. Toluene (200 ml) was added in this reaction solution. The organic layer was removed, and the aqueous layer was extracted with toluene. The organic layers were combined, washed with brine, and concentrated. The residue was evaporated under reduced pressure, and 2-ethoxy-1,7,8-trifluoronaphthalene was obtained.

후처리

  1. customThe organic layer was removed
  2. extractionthe aqueous layer was extracted with toluene
  3. washwashed with brine
  4. concentrationconcentrated
  5. customThe residue was evaporated under reduced pressure

출처 및 근거

ORD 기록
ord-c21c67302d004c128768a2f166002c3a
출처 데이터셋
uspto-grants-2007_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07214835B2

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