Water → 1-(Aminomethyl)cycloheptan-1-ol

HRID 424768노트

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HRID 424768 반응식
C[Si](C)(C)[O:3][C:4]1([C:11]#[N:12])[CH2:10][CH2:9][CH2:8][CH2:7][CH2:6][CH2:5]1.[H-].[Al+3].[Li+].[H-].[H-].[H-].O.[OH-].[Na+]>O1CCCC1>[NH2:12][CH2:11][C:4]1([OH:3])[CH2:10][CH2:9][CH2:8][CH2:7][CH2:6][CH2:5]1

참가 물질

6

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온도
12.5 °C

실험 절차

A solution of 1-[(trimethylsilyl)oxy]cycloheptanecarbonitrile (737.5 g) in tetrahydrofuran (738 ml) was charged to a vessel containing 1 molar lithium aluminium hydride solution in tetrahydrofuran (4980 ml) and tetrahydrofuran (369 ml) whilst maintaining the temperature at 55° C. to 60° C. Tetrahydrofuran (738 ml) was charged and the reaction stirred for 3 hours at 60° C. to 65° C. The reaction was cooled to 10 to 15° C. and charged with water (193 ml), premixed sodium hydroxide solution [water (389 ml), sodium hydroxide (69 g)], tetrahydrofuran (738 ml) and water (193 ml) maintaining the temperature at 15° C. to 25° C. The mixture was stirred for 70 minutes and filtered. The filter cake was washed with tetrahydrofuran (1476 ml) twice. The filtrates and washes were combined and charged to a reaction vessel and concentrated to ca. 1480 mL at 65° C. to 70° C. The mixture was cooled to 15° C. to 25° C. and transferred to a container with tetrahydrofuran (369 ml), to provide the title compound (381 g) as a colourless solution in tetrahydrofuran (1613 ml).

후처리

  1. temperaturewhilst maintaining the temperature at 55° C. to 60° C
  2. temperaturemaintaining the temperature at 15° C. to 25° C
  3. stirringThe mixture was stirred for 70 minutes
  4. filtrationfiltered
  5. washThe filter cake was washed with tetrahydrofuran (1476 ml) twice
  6. additioncharged to a reaction vessel
  7. concentrationconcentrated to ca. 1480 mL at 65° C. to 70° C
  8. temperatureThe mixture was cooled to 15° C. to 25° C.

출처 및 근거

ORD 기록
ord-f61ec715a2f64932966ff4086b70d9fa
출처 데이터셋
uspto-grants-2012_01
특허 번호
US08106073B2

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