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Trimellitic anhydride → 1,4-Dioxo-1,2,3,4-tetrahydrophthalazine-6-carboxylic acid

HRID 1783719
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인쇄 미리보기

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HRID 1783719 반응식
O.[NH2:2][NH2:3].[CH:4]1[C:9]([C:10]([OH:12])=[O:11])=[CH:8][C:7]2[C:13](O[C:16](=[O:17])[C:6]=2[CH:5]=1)=[O:14]>CC(O)=O>[O:17]=[C:16]1[C:6]2[C:7](=[CH:8][C:9]([C:10]([OH:12])=[O:11])=[CH:4][CH:5]=2)[C:13](=[O:14])[NH:3][NH:2]1
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참가 물질

4

반응물 2

HCID 11089Trimellitic anhydrideHCID 24654Hydrazine hydrate (1:1)

생성물 1

HCID 3090561,4-Dioxo-1,2,3,4-tetrahydrophthalazine-6-carboxylic acid수율 85%

시약·촉매·용매 1

HCID 176Acetic Acid용매

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온도
120 °C

실험 절차

Hydrazine hydrate (26 g, 0.52 mol) was added in one portion to a stirred mixture of 1,2,4-benzenetricarboxylic anhydride (100 g, 0.52 mol), in HOAc (1.0 L) at RT. The mixture was heated to 120° C. for 2 h and then allowed to cool to RT. The solid was filtered, washed with water (250 ml) and dried in the under vacuum at 50° C. for 20 hours to give the title compound (91 g, 85% yield).

후처리

  1. temperatureto cool to RT
  2. filtrationThe solid was filtered
  3. washwashed with water (250 ml)
  4. customdried in the under vacuum at 50° C. for 20 hours

출처 및 근거

ORD 기록
ord-4422387ee81c4337bcebf4753617b5b4
출처 데이터셋
uspto-grants-2009_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07501410B2

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