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Hydrazine hydrate (1:1) → 8-(4,5,6,7-Tetramethoxyindan-2-yl)octylamine

HRID 2268476
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HRID 2268476 반응식
[CH3:1][O:2][C:3]1[C:11]([O:12][CH3:13])=[C:10]([O:14][CH3:15])[C:9]([O:16][CH3:17])=[C:8]2[C:4]=1[CH2:5][CH:6]([CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][N:26]1C(=O)C3=CC=CC=C3C1=O)[CH2:7]2.O.NN>C(O)C>[CH3:17][O:16][C:9]1[C:10]([O:14][CH3:15])=[C:11]([O:12][CH3:13])[C:3]([O:2][CH3:1])=[C:4]2[C:8]=1[CH2:7][CH:6]([CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][NH2:26])[CH2:5]2
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참가 물질

4

반응물 2

HCID 24654Hydrazine hydrate (1:1)HCID 18348600N-[8-(4,5,6,7-tetramethoxyindan-2-yl)octyl]phthalimide

생성물 1

HCID 183485288-(4,5,6,7-Tetramethoxyindan-2-yl)octylamine수율 91.8%

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

The mixture of N-[8-(4,5,6,7-tetramethoxyindan-2-yl)octyl]phthalimide (384 mg), hydrazine monohydrate (194 mg) in ethanol (8 ml) was heated under reflux for 6 hr. The reaction mixture was cooled to room temperature and solid was filtered off and the filtrate was concentrated. The residue was diluted with ethyl acetate, washed with 1M aqueous potassium carbonate, water, and saturated aqueous sodium chloride, and dried. The solvent was removed in vacuo to yield the entitled compound (260 mg) as an oil.

후처리

  1. temperaturewas heated
  2. temperatureunder reflux for 6 hr
  3. filtrationsolid was filtered off
  4. concentrationthe filtrate was concentrated
  5. additionThe residue was diluted with ethyl acetate
  6. washwashed with 1M aqueous potassium carbonate, water, and saturated aqueous sodium chloride
  7. customdried
  8. customThe solvent was removed in vacuo

출처 및 근거

ORD 기록
ord-904bc13e562e495a9b4be68fed61e858
출처 데이터셋
uspto-grants-2001_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06326369B1

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