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

HRID 1910556
ノート
印刷プレビュー

反応式

HRID 1910556 の反応式
[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]
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 284Formic AcidHCID 713FormamideHCID 3283Diethyl EtherHCID 69144Isobutyrophenone

生成物 1

HCID 49628752-Methyl-1-phenylpropan-1-amine収率 61%

試薬・触媒・溶媒 1

HCID 962Water溶媒

実験手順

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).

後処理

  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

出典と根拠

ORDレコード
ord-ac536126eda5431a836e1913d120fce7
出典データセット
uspto-grants-2013_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08604021B2

反応ノート

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