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HCID 58194293, 화합물 → HCID 58194347, 화합물

HRID 68526
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HRID 68526 반응식
[CH:1]1[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH:4]=[CH:3][C:2]=1[C:11]1[CH:12]=[C:13]([CH:25]=[CH:26][CH:27]=1)[C:14]([C:16]1[CH:24]=[CH:23][CH:22]=[CH:21][C:17]=1[C:18]([OH:20])=[O:19])=O>[OH-].[Na+].[Zn].S([O-])([O-])(=O)=O.[Cu+2]>[CH:1]1[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH:4]=[CH:3][C:2]=1[C:11]1[CH:12]=[C:13]([CH:25]=[CH:26][CH:27]=1)[CH2:14][C:16]1[CH:24]=[CH:23][CH:22]=[CH:21][C:17]=1[C:18]([OH:20])=[O:19]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 1

HCID 58194293HCID 58194293, 화합물

생성물 1

HCID 58194347HCID 58194347, 화합물수율 94.7%

시약·촉매·용매 3

HCID 23994Zinc촉매HCID 24462Copper Sulfate촉매HCID 14798Sodium Hydroxide용매

실험 절차

First, 121 g of 2-[3-(2-naphthyl)benzoyl]benzoic acid were dissolved in 10 L of a 1N sodium hydroxide solution, and then a zinc powder activated with an aqueous solution of copper sulfate was added to the solution. The reaction solution was stirred for 50 hours under reflux. After having been cooled to room temperature, the reaction solution was filtrated. The filtrate was acidified, and then the resultant solid was washed with boiling water. Thus, 110 g of 2-[3-(2-naphthyl)benzyl]benzoic acid were obtained (in 90% yield).

후처리

  1. additionwas added to the solution
  2. temperatureunder reflux
  3. filtrationthe reaction solution was filtrated
  4. washthe resultant solid was washed with boiling water

출처 및 근거

ORD 기록
ord-26e34821b2e84db6980d9c9b618027e3
출처 데이터셋
uspto-grants-2014_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08822041B2

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