Sodium Hydroxide → HCID 21412125, compound

HRID 2071716Notes

Reaction equation

HRID 2071716 reaction equation
[C:1]([NH:4][CH2:5][CH2:6][CH:7]=[C:8]1[C:14]2[CH:15]=[CH:16][CH:17]=[CH:18][C:13]=2[CH:12]=[CH:11][C:10]2[CH:19]=[CH:20][CH:21]=[CH:22][C:9]1=2)(=O)[CH3:2].[H-].[Al+3].[Li+].[H-].[H-].[H-].[H-].[OH-].[Na+]>CCOCC.O>[CH2:1]([NH:4][CH2:5][CH2:6][CH:7]=[C:8]1[C:14]2[CH:15]=[CH:16][CH:17]=[CH:18][C:13]=2[CH:12]=[CH:11][C:10]2[CH:19]=[CH:20][CH:21]=[CH:22][C:9]1=2)[CH3:2]

Participants

7

Procedure

5-(3-Acetamidopropylidene)-5H-dibenzo[a,d]cycloheptene is dissolved in absolute ether. The solution is added dropwise to a stirred solution of lithium aluminum hydride in ether, containing 1.25 molar equivalents of the hydride. The mixture is stirred for 2 hours at room temperature, then for 15 hours at reflux. The mixture is then cooled and stirred while water is added cautiously, followed by sodium hydroxide solution. The ether layer is separated, washed with water and dried over sodium sulfate. The product is obtained by evaporation of the ether and purified by vacuum distillation.

Workup

  1. temperaturefor 15 hours at reflux
  2. temperatureThe mixture is then cooled
  3. additionis added cautiously
  4. customThe ether layer is separated
  5. washwashed with water
  6. dry with materialdried over sodium sulfate
  7. customThe product is obtained by evaporation of the ether
  8. distillationpurified by vacuum distillation

Sources & evidence

ORD record
ord-be6d0498584b49c6a405f34f27b0cc11
Source dataset
uspto-grants-1977_09
Patent number
US04048223

Reaction notes

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