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1-Diphenylmethoxy-2-formylamino-2-methylpropane → 1-Diphenylmethoxy-2-methyl-2-(methylamino)propane

HRID 1613189
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HRID 1613189 반응식
[C:1]1([CH:7]([C:16]2[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=2)[O:8][CH2:9][C:10]([NH:13][CH:14]=O)([CH3:12])[CH3:11])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[H-].[Al+3].[Li+].[H-].[H-].[H-]>CCOCC>[C:1]1([CH:7]([C:16]2[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=2)[O:8][CH2:9][C:10]([CH3:12])([NH:13][CH3:14])[CH3:11])[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 197753101-Diphenylmethoxy-2-formylamino-2-methylpropaneHCID 21226445Aluminium lithium hydride

생성물 1

HCID 197753221-Diphenylmethoxy-2-methyl-2-(methylamino)propane수율 96.2%

시약·촉매·용매 1

HCID 3283Diethyl Ether용매2회

실험 절차

A solution of 1-diphenylmethoxy-2-formylamino-2-methylpropane (8.2 g) in ether (50 ml) was added to a suspension of lithium aluminium hydride (2.2 g) in ether (100 ml) at a rate which maintained a gentle reflux. The mixture was stirred at room temperature for 18 hours, quenched by the sequential dropwise addition of water (2.2 ml), 5M aqueous sodium hydroxide solution (2.2 ml) and water (6.6 ml) and filtered. The filtrate was dried over sodium sulphate and evaporated to give the title compound as a colourless gum (7.5 g, 96%).

후처리

  1. temperaturemaintained a gentle reflux
  2. customquenched by the sequential dropwise addition of water (2.2 ml), 5M aqueous sodium hydroxide solution (2.2 ml) and water (6.6 ml)
  3. filtrationfiltered
  4. dry with materialThe filtrate was dried over sodium sulphate
  5. customevaporated

출처 및 근거

ORD 기록
ord-5701b48055a04608996cfde911c2e71b
출처 데이터셋
uspto-grants-1993_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05192765

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