HCID 178418255, compound → 1,2,3,5-Tetrahydro-7-phenyl-s-indacene

HRID 276738Notes

Reaction equation

HRID 276738 reaction equation
[C:1]1([Mg]Br)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1>C(OCC)C>[C:1]1([C:2]2[C:2]3[CH:3]=[C:4]4[C:5]([CH2:3][CH2:4][CH2:5]4)=[CH:6][C:1]=3[CH2:6][CH:1]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1

Participants

3

Reactant 1

HCID 178418255HCID 178418255, compound

Product 1

HCID 186283771,2,3,5-Tetrahydro-7-phenyl-s-indaceneYield 90.3%

Reagents, catalysts & solvents 1

HCID 3283Diethyl EtherSolvent

Procedure

3,5,6,7-Tetrahydro-s-Hydrindacen-1(2H)-one (12.00 g, 0.06967 moles) was stirred in diethyl ether (200 mL) at 0° C. as PhMgBr (0.1 05 moles, 35.00 mL of 3.0 M solution in diethyl ether) was added slowly. This mixture was then allowed to stir overnight at room temperature. After the reaction period the mixture was quenched by pouring over ice. The mixture was then acidified (pH=1) with HCl and stirred vigorously for 2 hours. The organic layer was then separated and washed with H2O (2×100 mL) and then dried over MgSO4. Filtration followed by the removal of the volatiles resulted in the isolation of the desired product as a dark oil (14.68 g, 90.3% yield).

Workup

  1. additionwas added slowly
  2. customAfter the reaction period the mixture
  3. customwas quenched
  4. additionby pouring over ice
  5. stirringstirred vigorously for 2 hours
  6. customThe organic layer was then separated
  7. washwashed with H2O (2×100 mL)
  8. dry with materialdried over MgSO4
  9. filtrationFiltration
  10. customfollowed by the removal of the volatiles

Sources & evidence

ORD record
ord-67707457cd1b4ec1aafa2e6f47727c29
Source dataset
uspto-grants-2002_03
Patent number
US06355341B1

Reaction notes

Loading…