5-Azido-5-(2-methoxyphenyl)-1-pentene → 5-Amino-5-(2-methoxyphenyl)-1-pentene

HRID 377156Notes

Reaction equation

HRID 377156 reaction equation
[N:1]([CH:4]([C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][C:10]=1[O:15][CH3:16])[CH2:5][CH2:6][CH:7]=[CH2:8])=[N+]=[N-].[H-].[H-].[H-].[H-].[Li+].[Al+3]>CCOCC>[NH2:1][CH:4]([C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][C:10]=1[O:15][CH3:16])[CH2:5][CH2:6][CH:7]=[CH2:8]

Participants

4

Procedure

To a solution of 5-azido-5-(2-methoxyphenyl)-1-pentene (1.59 g. 7.33 mmol) in anhydrous ether (10 mL) at 0° C. was added to LiAlH4 in diethyl ether (1.OM, 7.33 mL) dropwise over a period of 20 minutes. The ice bath was removed and the reaction mixture was kept at room temperature for 25 minutes. The reaction solution was cooled to 0° C. to 40° C. and saturated Na2SO4 solution was added dropwise until no hydrogen gas was evolved. Anhydrous Na2SO4 was added followed by diethyl ether (70 mL), the resulting suspension was stirred at room temperature for 1 hour and the solution was then filtered through a pad of Celite™. The filtrate was evaporated to give the title compound (1.63 g) as a colorless oil, which was used for the Preparation 19 without purification. 1H NMR (CDCl3, 400 MHz)δ: 7.22 (2H), 6.93 (3H), 5.80 (1H), 4.92 (2H), 4.13 (1H), 3.82 (3H, OMe), 1.2-2.2 (6H).

Workup

  1. customThe ice bath was removed
  2. temperatureThe reaction solution was cooled to 0° C. to 40° C.
  3. additionsaturated Na2SO4 solution was added dropwise until no hydrogen gas
  4. additionAnhydrous Na2SO4 was added
  5. filtrationthe solution was then filtered through a pad of Celite™
  6. customThe filtrate was evaporated

Sources & evidence

ORD record
ord-a2968436c5ba47ffaab5a6c5270745c4
Source dataset
uspto-grants-2000_02
Patent number
US06025350

Reaction notes

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