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Hydrochloric Acid → HCID 67459068, 화합물

HRID 554526
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HRID 554526 반응식
C([O:8][C:9]1[CH:14]=[C:13]([F:15])[CH:12]=[CH:11][C:10]=1[CH:16]([C:18]1[CH:23]=[CH:22][C:21]([O:24][CH3:25])=[CH:20][CH:19]=1)O)C1C=CC=CC=1.Cl>CO.[OH-].[Pd+2].[OH-]>[CH3:25][O:24][C:21]1[CH:20]=[CH:19][C:18]([CH2:16][C:10]2[CH:11]=[CH:12][C:13]([F:15])=[CH:14][C:9]=2[OH:8])=[CH:23][CH:22]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 313Hydrochloric AcidHCID 67461295HCID 67461295, 화합물

생성물 1

HCID 67459068HCID 67459068, 화합물수율 34%

시약·촉매·용매 2

HCID 9942167Palladium hydroxide촉매HCID 887Methanol용매

실험 절차

To a solution of (2-benzyloxy-4-fluorophenyl)-(4-methoxyphenyl)-methanol (2.095 g, 6.19 mmol) in methanol (20 mL), a 20% palladium hydroxide catalyst (200 mg) was added and furthermore 2N—HCl (0.3 mL) was added thereto. The mixture was stirred under a hydrogen atmosphere for 16 hours, and then the catalyst was filtered off. The solvent was distilled under reduced pressure, and the obtained residue was purified by silica gel column chromatography [developing solution=ethyl acetate:n-hexane (1:5)] to obtain the title compound (489 mg, 34%).

후처리

  1. filtrationthe catalyst was filtered off
  2. distillationThe solvent was distilled under reduced pressure
  3. customthe obtained residue was purified by silica gel column chromatography [developing solution=ethyl acetate:n-hexane (1:5)]

출처 및 근거

ORD 기록
ord-9c8ba01b4b314edca61d2fc38945bf10
출처 데이터셋
uspto-grants-2011_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08048897B2

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