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Sodium Hydroxide → 6-nitro-1H-indole-2-carboxylic Acid

HRID 724537
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HRID 724537 반응식
C[O:2][C:3]([C:5]1[NH:6][C:7]2[C:12]([CH:13]=1)=[CH:11][CH:10]=[C:9]([N+:14]([O-:16])=[O:15])[CH:8]=2)=[O:4].[OH-].[Na+]>CO>[N+:14]([C:9]1[CH:8]=[C:7]2[C:12]([CH:13]=[C:5]([C:3]([OH:4])=[O:2])[NH:6]2)=[CH:11][CH:10]=1)([O-:16])=[O:15]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 14798Sodium HydroxideHCID 11816863Methyl 6-nitro-1H-indole-2-carboxylate

생성물 1

HCID 47149976-nitro-1H-indole-2-carboxylic Acid수율 95.1%

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

4.4 g (20 mmol) 6-Nitro-1H-indole-2-carboxylic acid methyl ester (190) was dissolved in 80 mL methanol and was treated with 30 mL 1M NaOH overnight at 55 C°. The methanol was evaporated, the remaining aqueous solution was diluted to 100 mL and was acidified to pH 2 using concentrated HCl. The precipitate was filtered off, washed three times with water then dried to give 3.92 g (95%) 191 as yellow powder. The NMR was consistent with the structure. 191 was used without further purification.

후처리

  1. customThe methanol was evaporated
  2. additionthe remaining aqueous solution was diluted to 100 mL
  3. filtrationThe precipitate was filtered off
  4. washwashed three times with water
  5. customthen dried

출처 및 근거

ORD 기록
ord-b9e48dbd07354afeaca14050f1d6aff6
출처 데이터셋
uspto-grants-2006_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07141680B2

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