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Water → HCID 14012545, 화합물

HRID 568693
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HRID 568693 반응식
[H-].[Al+3].[Li+].[H-].[H-].[H-].C([O:9][C:10](=O)[CH2:11][O:12][C:13]1[CH:28]=[CH:27][C:16]2[C:17]([C:20]3[CH:25]=[CH:24][CH:23]=[CH:22][C:21]=3[F:26])=[N:18][O:19][C:15]=2[C:14]=1[Cl:29])C.O.[OH-].[Na+]>CCOCC>[Cl:29][C:14]1[C:15]2[O:19][N:18]=[C:17]([C:20]3[CH:25]=[CH:24][CH:23]=[CH:22][C:21]=3[F:26])[C:16]=2[CH:27]=[CH:28][C:13]=1[O:12][CH2:11][CH2:10][OH:9]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 962Water2회HCID 14798Sodium HydroxideHCID 13015713HCID 13015713, 화합물HCID 21226445Aluminium lithium hydride

생성물 1

HCID 14012545HCID 14012545, 화합물

시약·촉매·용매 1

HCID 3283Diethyl Ether용매2회

실험 절차

To a suspension of 0.9 g lithium aluminum hydride (98%) in 100 ml anhydrous ether is added a solution of 10 g ethyl-2-{[7-chloro-3-(2-fluorophenyl)-1,2-benzisoxazole-6-yl]oxy}acetate of Example 1d in 200 ml ether containing sufficient tetrahydrofuran to effect solution. The reaction mixture is stirred for two hours at room temperature and one hour at reflux. To the reaction mixture is added 0.9 ml H2O, 0.9 ml 15% NaOH and 2.7 ml H2O. The stirred suspension is filtered and the filtrate is concentrated to afford 2-{[7-chloro-3-(2-fluorophenyl)-1,2-benzisoxazole-6-yl]oxy}ethanol, mp 112° C.

후처리

  1. temperatureat reflux
  2. filtrationThe stirred suspension is filtered
  3. concentrationthe filtrate is concentrated

출처 및 근거

ORD 기록
ord-2fc2e5e63fe441e69b1977aaddd1617b
출처 데이터셋
uspto-grants-1988_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04728662

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