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Hydrazine hydrate (1:1) → 3-(4-Chlorophenoxy-methyl)-benzylamine

HRID 2097355
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HRID 2097355 반응식
[Cl:1][C:2]1[CH:27]=[CH:26][C:5]([O:6][CH2:7][C:8]2[CH:9]=[C:10]([CH:23]=[CH:24][CH:25]=2)[CH2:11]C23C=CC=CC2C(NC3=O)=O)=[CH:4][CH:3]=1.O.[NH2:29]N>C1COCC1.CCO>[Cl:1][C:2]1[CH:27]=[CH:26][C:5]([O:6][CH2:7][C:8]2[CH:9]=[C:10]([CH:23]=[CH:24][CH:25]=2)[CH2:11][NH2:29])=[CH:4][CH:3]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 24654Hydrazine hydrate (1:1)HCID 231324422-[3-(4-Chloro-phenoxymethyl)-benzyl]-phthalimide

생성물 1

HCID 231324473-(4-Chlorophenoxy-methyl)-benzylamine

시약·촉매·용매 2

HCID 702Ethanol용매HCID 8028Tetrahydrofuran용매

실험 절차

2-[3-(4-Chloro-phenoxymethyl)-benzyl]-phthalimide (345 mg, 0.91 mmol) and hydrazine hydrate (0.27 mL, 4.5 mmol) were dissolved in THF (2.5 mL) and EtOH (2.5 mL). The mixture was heated to reflux for 17 h, cooled to r.t. and evaporated to dryness. The residue was suspended in THF (6 mL). The precipitate was filtered and washed with THF (4×3 mL). The filtrate was evaporated to dryness to give the title compound, pure enough for further reactions.

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후처리

  1. temperatureThe mixture was heated
  2. temperatureto reflux for 17 h
  3. customevaporated to dryness
  4. filtrationThe precipitate was filtered
  5. washwashed with THF (4×3 mL)
  6. customThe filtrate was evaporated to dryness

출처 및 근거

ORD 기록
ord-d7f38881d3e64a7f93546eedaabfd339
출처 데이터셋
uspto-grants-2013_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08450348B2

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