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Sodium Hydroxide → HCID 58840902, 화합물

HRID 1162287
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반응식

HRID 1162287 반응식
C[O:2][C:3](=[O:22])[CH:4]([O:11][C:12]([NH:14][C:15]1[CH:20]=[CH:19][C:18]([Cl:21])=[CH:17][CH:16]=1)=[O:13])[C:5]1[CH:10]=[CH:9][CH:8]=[CH:7][CH:6]=1.[OH-].[Na+]>CO.C1COCC1>[Cl:21][C:18]1[CH:19]=[CH:20][C:15]([NH:14][C:12]([O:11][CH:4]([C:5]2[CH:6]=[CH:7][CH:8]=[CH:9][CH:10]=2)[C:3]([OH:22])=[O:2])=[O:13])=[CH:16][CH:17]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 14798Sodium HydroxideHCID 86612126HCID 86612126, 화합물

생성물 1

HCID 58840902HCID 58840902, 화합물수율 89%

시약·촉매·용매 2

HCID 887Methanol용매HCID 8028Tetrahydrofuran용매

실험 절차

Methyl((((4-chlorophenyl)amino)carbonyl)oxy)(phenyl)acetate (0.73 g) obtained in Example 3a) and 1 N sodium hydroxide (3.0 ml) were dissolved in methanol (10 ml) and THF (10 ml), and then mixed at room temperature for 15 hours. The reaction solution was then concentrated under reduced pressure, acidified by adding 1 N hydrochloric acid to the concentrated solution, and then the precipitate was collected by filtration and washed with water to obtain the title compound as pale brown powder (0.62 g, 89%).

후처리

  1. concentrationThe reaction solution was then concentrated under reduced pressure
  2. additionby adding 1 N hydrochloric acid to the concentrated solution
  3. filtrationthe precipitate was collected by filtration
  4. washwashed with water

출처 및 근거

ORD 기록
ord-786dfc72404a4c80b489fbbe08235b99
출처 데이터셋
uspto-grants-2010_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07820673B2

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