Sodium Hydroxide → HCID 21412125, compound

HRID 1284228Notes

Reaction equation

HRID 1284228 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-c754133d85ea40f690cec36b52ff3521
Source dataset
uspto-grants-1976_08
Patent number
US03978121

Reaction notes

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