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Sodium Hydroxide → 6,7-Dimethoxy-2-methoxyimino-1,2,3,4-Tetrahydronaphthalene

HRID 1446926
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HRID 1446926 반응식
Cl.[O:2]([NH2:4])[CH3:3].[OH-].[Na+].[CH3:7][O:8][C:9]1[CH:10]=[C:11]2[C:16](=[CH:17][C:18]=1[O:19][CH3:20])[CH2:15][C:14](=O)[CH2:13][CH2:12]2>O>[CH3:20][O:19][C:18]1[CH:17]=[C:16]2[C:11](=[CH:10][C:9]=1[O:8][CH3:7])[CH2:12][C:13](=[N:4][O:2][CH3:3])[CH2:14][CH2:15]2
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 14798Sodium HydroxideHCID 521874O-Methylhydroxylamine hydrochlorideHCID 6098446,7-Dimethoxy-2-tetralone

생성물 1

HCID 538187636,7-Dimethoxy-2-methoxyimino-1,2,3,4-Tetrahydronaphthalene수율 89.2%

시약·촉매·용매 1

HCID 962Water용매

실험 절차

A mixture of 0.56 g (6.7 mmol) of methoxylamine hydrochloride and 6.5 ml (6.5 mmol) of a 1 M aqueous solution of NaOH was added to 0.689 g (3.34 mmol) of 6,7-dimethoxy-2-tetralone (IV). While under a nitrogen atmosphere the mixture was warmed to ca. 100° for 15 minutes and then kept at 40° using an infrared lamp for 18 hours. Water was added to the mixture which was then extracted with ether. The combined extracts were dried (MgSO4) and the solvent was removed on a rotary evaporator, affording 0.700 g (89.2%) of brown oil: nmr (CDCl3) δ2.3-2.9 (m, 4H), 3.32 (S, 1H), 3.57 (S, 1H), 3.73 (S, 6H), 3.78 (S, 3H), 6.4-6.6 (m, 2H). The compound was used without further purification.

후처리

  1. temperatureWhile under a nitrogen atmosphere the mixture was warmed to ca. 100° for 15 minutes
  2. customkept at 40°
  3. customfor 18 hours
  4. extractionwas then extracted with ether
  5. dry with materialThe combined extracts were dried (MgSO4)
  6. customthe solvent was removed on a rotary evaporator

출처 및 근거

ORD 기록
ord-3c3e5cc9851641b5adce9db45e0fd9a1
출처 데이터셋
uspto-grants-1982_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04314082

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