Ethanol → 2-Methyl-2,3,3a,8-tetrahydro-dibenzo [1,2:5,6]cyclohepta[3,4-c]pyrrole

HRID 1680036Notes

Reaction equation

HRID 1680036 reaction equation
[CH3:1][N:2]1[CH2:6][C@@H:5]2[C:7]3[CH:19]=[CH:18][CH:17]=[CH:16][C:8]=3[CH2:9][C:10]3[CH:15]=[CH:14][CH:13]=[CH:12][C:11]=3[C@@H:4]2[C:3]1=O.[H-].[H-].[H-].[H-].[Li+].[Al+3].O.C(O)C>CCOCC.O1CCCC1.CCOCC>[CH3:1][N:2]1[CH2:6][CH:5]2[C:7]3[CH:19]=[CH:18][CH:17]=[CH:16][C:8]=3[CH2:9][C:10]3[CH:15]=[CH:14][CH:13]=[CH:12][C:11]=3[C:4]2=[CH:3]1

Participants

7

Reactant 4

HCID 702EthanolHCID 962WaterHCID 21226445Aluminium lithium hydrideHCID 86736413cis-2-methyl-3,3a,8,12b-tetrahydro-dibenzo[1,2;5,6]cyclohepta[3,4-c]pyrrol-1(2H)-one

Product 1

HCID 705722482-Methyl-2,3,3a,8-tetrahydro-dibenzo [1,2:5,6]cyclohepta[3,4-c]pyrroleYield 38%

Reagents, catalysts & solvents 2

HCID 3283Diethyl EtherSolventHCID 21868444Ether tetrahydrofuranSolvent

Procedure

0.7 g cis-2-methyl-3,3a,8,12b-tetrahydro-dibenzo [1,2;5,6]cyclohepta[3,4-c]pyrrol-1(2H)-one is dissolved in 25 ml dry ether/tetrahydrofuran (1:1). This solution is slowly added at 0° C. to a suspension of 0.35 g LiAlH4 in 20 ml ether/t.h.f. (1.1). After stirring for 15 minutes, water is added and the mixture is then filtered. The filtrate is subsequently evaporated to dryness under vacuum. This gives an oily residue, weighting about 0.7 g. Addition of 8 ml ethanol to this residue results in the formation of a precipitate, which is filtered off. [The crystalline product thus obtained is recrystallized, giving 0.25 g 2-methyl-2,3,3a,8-tetrahydro-dibenzo [1,2;5,6]cyclohepta[3,4-c]pyrrole of melting point 128°-131° C. (=enamine according to formula III)].

Workup

  1. filtrationthe mixture is then filtered
  2. customThe filtrate is subsequently evaporated to dryness under vacuum
  3. customThis gives an oily residue
  4. customresults in the formation of a precipitate, which
  5. filtrationis filtered off
  6. custom[The crystalline product thus obtained
  7. customis recrystallized

Sources & evidence

ORD record
ord-b8d60147aa8243fd933a9d949b2e36d9
Source dataset
uspto-grants-1981_06
Patent number
US04271179

Reaction notes

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