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Water → HCID 70637164, compound

HRID 1658719
Notes
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Reaction equation

HRID 1658719 reaction equation
[H-].[H-].[H-].[H-].[Li+].[Al+3].[C:7]([CH:9]1[CH2:27][CH2:26][N:12]2[C:13]3[CH:25]=[CH:24][CH:23]=[CH:22][C:14]=3[CH2:15][C:16]3[CH:21]=[CH:20][CH:19]=[CH:18][C:17]=3[CH:11]2[CH2:10]1)#[N:8].O>CCOCC.C1COCC1>[NH2:8][CH2:7][CH:9]1[CH2:27][CH2:26][N:12]2[C:13]3[CH:25]=[CH:24][CH:23]=[CH:22][C:14]=3[CH2:15][C:16]3[CH:21]=[CH:20][CH:19]=[CH:18][C:17]=3[CH:11]2[CH2:10]1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

6

Reactant 3

HCID 962WaterHCID 21226445Aluminium lithium hydride2×HCID 70637584HCID 70637584, compound

Product 1

HCID 70637164HCID 70637164, compound

Reagents, catalysts & solvents 2

HCID 3283Diethyl EtherSolventHCID 8028Tetrahydrofuran
Solvent

Procedure

To a suspension of 10 g LiAlH4 in 400 ml of dry ether a solution of 8 g of 2-cyano-1,2,3,4,10,14b-hexahydro-pyridino[1,2-a]-dibenzo[c,f]-azepine (axial) in 300 ml of THF is added. Then the mixture is refluxed for 30 minutes, whereupon it is cooled by means of ice. After that 40 ml of water are added to the mixture carefully so as to hydrolyse the excess of LiAlH4. The resulting precipitate is filtered off after which the filtrate is evaporated.

Workup

  1. additionis added
  2. temperatureThen the mixture is refluxed for 30 minutes, whereupon it
  3. temperatureis cooled by means of ice
  4. filtrationThe resulting precipitate is filtered off after which the filtrate
  5. customis evaporated

Sources & evidence

ORD record
ord-8884fb94fc8d456c8a067523bb01c1de
Source dataset
uspto-grants-1976_06
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US03966723

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes