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Ethanol → HCID 23248654, 화합물

HRID 1739831
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HRID 1739831 반응식
[N+:1]([C:4]1[CH:9]=[CH:8][C:7]([CH:10]2[O:14][CH2:13][CH2:12][O:11]2)=[CH:6][CH:5]=1)([O-:3])=O.[Cl:15][C:16]1[CH:17]=[C:18]([CH2:22]C#N)[CH:19]=[CH:20][CH:21]=1.[OH-].[Na+].[CH2:27](O)[CH3:28]>CO>[Cl:15][C:16]1[CH:17]=[C:18]([C:22]2[O:3][N:1]=[C:4]3[CH:9]=[CH:8][C:7]([C:10]4([C:28]5[CH:27]=[CH:17][C:16]([Cl:15])=[CH:21][CH:20]=5)[O:14][CH2:13][CH2:12][O:11]4)=[CH:6][C:5]=23)[CH:19]=[CH:20][CH:21]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 702EthanolHCID 14798Sodium HydroxideHCID 73722m-ChlorophenylacetonitrileHCID 2667962-(4-Nitrophenyl)-1,3-dioxolane

생성물 1

HCID 23248654HCID 23248654, 화합물수율 86%

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

Interm. (7-a) (50 g) and then (3-chlorophenyl)acetonitrile (34.8 ml) were added to a mixture of sodium hydroxide (32.8 g) in methanol (100 ml). The mixture was stirred and refluxed till complete dissolution. The reaction was carried out twice with the same quantities. The mixtures were combined. Ice and then ethanol were added. The mixture was allowed to crystallize out. The precipitate was filtered off, washed with ethanol and dried, yielding 58 g (86%) of 3-(3-chlorophenyl)-5-[2-(4-chlorophenyl)-1,3-dioxolan-2-yl]-2,1-benzisoxazole (interm. 9-a).

후처리

  1. temperaturerefluxed till complete dissolution
  2. customto crystallize out
  3. filtrationThe precipitate was filtered off
  4. washwashed with ethanol
  5. customdried

출처 및 근거

ORD 기록
ord-d23e0d77e6d3456199b6482e9e3473a4
출처 데이터셋
uspto-grants-1999_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05968952

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