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Oxalyl chloride → HCID 71556273, 화합물

HRID 929486
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반응식

HRID 929486 반응식
O[C:2]1[C:3](=[O:20])[N:4]([C:14]2[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=2)[C:5](=[O:13])[C:6]=1[C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=1.C(Cl)(=O)C([Cl:24])=O>CN(C=O)C>[Cl:24][C:2]1[C:3](=[O:20])[N:4]([C:14]2[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=2)[C:5](=[O:13])[C:6]=1[C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 65578Oxalyl chlorideHCID 546840203-hydroxy-1,4-diphenyl-1H-pyrrole-2,5-dione

생성물 1

HCID 71556273HCID 71556273, 화합물

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

After dissolving compound 6a (2.00 g, 7.54 mmol) in MC (10 ml) and anhydrous DMF (10 ml), oxalyl chloride (1.90 g, 15.0 mmoL) was added thereto and the agitation for 30 minutes was carried out. After the identification of the reaction progress with TLC, the reaction was terminated. Then, three times extractions were carried out with EA and three times washings were carried out with brine. Water was removed by using Na2SO4, solvents were removed and then, the column chromatography was carried out with EA/HX ( 1/9). As the result, Compound 7a was obtained.

후처리

  1. additionwas added
  2. customAfter the identification of the reaction progress with TLC, the reaction was terminated
  3. extractionThen, three times extractions
  4. customWater was removed
  5. customwere removed

출처 및 근거

ORD 기록
ord-b842b4e7ae044cd4b8d59770d6bcedb5
출처 데이터셋
uspto-grants-2016_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09296690B2

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