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Formic Acid → 2-Methyl-1-phenylpropan-1-amine

HRID 1910556
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HRID 1910556 반응식
[C:1]([C:6]1[CH:11]=[CH:10][CH:9]=[CH:8][CH:7]=1)(=O)[CH:2]([CH3:4])[CH3:3].C(O)=O.C(OCC)C.C([NH2:22])=O>O>[CH3:3][CH:2]([CH3:4])[CH:1]([C:6]1[CH:11]=[CH:10][CH:9]=[CH:8][CH:7]=1)[NH2:22]
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참가 물질

6

반응물 4

HCID 284Formic AcidHCID 713FormamideHCID 3283Diethyl EtherHCID 69144Isobutyrophenone

생성물 1

HCID 49628752-Methyl-1-phenylpropan-1-amine수율 61%

시약·촉매·용매 1

HCID 962Water용매

실험 절차

A solution of isobutyrophenone (5.1 mL, 33.7 mmol) and formic acid (1.3 mL, 33.7 mmol) in formamide was stirred at 165-180° C. for 20 h. The mixture was cooled, diluted with water, and extracted with benzene. The benzene was concentrated down and the residue was boiled in 3 M HCl (10 mL) for 48 h. The cooled reaction mixture was added to diethyl ether and extracted with water. The combined water extracts were basified with 20% NaOH, and extracted with dichloromethane. The combined extracts were washed with brine, dried (Na2SO4) and concentrated in vacuo to yield 3.09 g (61%) of the desired amine: 1H NMR (400 MHz, CD3OD): δ 7.33-7.23 (m, 4H), 7.22-7.20 (m, 1H), 3.49 (d, 1H), 1.87 (m, 1H), 1.00 (d, 3H), 0.73 (d, 3H). MS (ESI) m/z: Calculated: 149.12; Observed: 149.9 (M++1).

후처리

  1. temperatureThe mixture was cooled
  2. extractionextracted with benzene
  3. concentrationThe benzene was concentrated down
  4. customThe cooled reaction mixture
  5. extractionextracted with water
  6. extractionextracted with dichloromethane
  7. washThe combined extracts were washed with brine
  8. dry with materialdried (Na2SO4)
  9. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-ac536126eda5431a836e1913d120fce7
출처 데이터셋
uspto-grants-2013_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08604021B2

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