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Water → (2-(Aminomethyl)phenyl)methanol

HRID 1859412
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HRID 1859412 반응식
[H-].[Al+3].[Li+].[H-].[H-].[H-].[C:7]([CH2:9][C:10]1C=C[CH:16]=[CH:15][C:11]=1C([O-])=O)#[N:8].O.[OH-].[Na+].C([O:24][CH2:25][CH3:26])C>>[OH:24][CH2:25][C:26]1[CH:16]=[CH:15][CH:11]=[CH:10][C:9]=1[CH2:7][NH2:8]
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참가 물질

6

반응물 5

HCID 962Water2회HCID 3283Diethyl EtherHCID 14798Sodium HydroxideHCID 69851902-(Cyanomethyl)benzoateHCID 21226445Aluminium lithium hydride

생성물 1

HCID 11275036(2-(Aminomethyl)phenyl)methanol

실험 절차

Lithium aluminium hydride (12.4 ml, 1.0M in diethyl ether) was added cautiously to 2-cyanomethylbenzoate (1.00 g, 6.2 mmol) in anhydrous diethyl ether (40 ml) under nitrogen with stirring over 10 min. whilst ensuring the temperature was not greater than 15-25° C. using an ice bath. After the addition was complete the reaction mixture was allowed to warm to 21 C and then heated at reflux for 16 h. The reaction mixture was cooled to approximately −10 C. It was treated cautiously dropwise with water (0.5 ml), 20% aqueous sodium hydroxide (0.37 ml) and water (1.74 ml). The resultant green heterogeous mixture was filtered and the residue was with diethyl ether (150 ml), the combined washings and filtrate were dried (MgSO4) and solvent was removed in vacuo affording the title compound as a green oil (0.807 g). Mass Spectrum m/z 138 (MH+ for C8H12NO).

후처리

  1. customwas not greater than 15-25° C.
  2. additionAfter the addition
  3. temperatureto warm to 21 C
  4. temperatureheated
  5. temperatureat reflux for 16 h
  6. temperatureThe reaction mixture was cooled to approximately −10 C
  7. filtrationThe resultant green heterogeous mixture was filtered
  8. dry with materialthe combined washings and filtrate were dried (MgSO4) and solvent
  9. customwas removed in vacuo

출처 및 근거

ORD 기록
ord-416b308d59df4b478e7a9dc75661c0a6
출처 데이터셋
uspto-grants-2003_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06528494B2

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