1,1-Dichloroethane → HCID 58026943, compound

HRID 1966303Notes

Reaction equation

HRID 1966303 reaction equation
[Cl-].[Al+3].[Cl-].[Cl-].ClC(Cl)C.[C:9]1([CH2:15][C:16](Cl)=[O:17])[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=1.[CH3:19][O:20][C:21]1[CH:26]=[CH:25][CH:24]=[CH:23][C:22]=1[C:27]1[C:28]([CH2:40][O:41][C:42](=[O:50])[C:43]2[CH:48]=[CH:47][C:46]([CH3:49])=[CH:45][CH:44]=2)=[C:29]2[C:34](=[CH:35][CH:36]=1)[NH:33][C:32]([CH3:38])([CH3:37])[CH:31]=[C:30]2[CH3:39]>C(OCC)(=O)C>[CH3:19][O:20][C:21]1[CH:26]=[CH:25][C:24]([C:16](=[O:17])[CH2:15][C:9]2[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=2)=[CH:23][C:22]=1[C:27]1[C:28]([CH2:40][O:41][C:42](=[O:50])[C:43]2[CH:48]=[CH:47][C:46]([CH3:49])=[CH:45][CH:44]=2)=[C:29]2[C:34](=[CH:35][CH:36]=1)[NH:33][C:32]([CH3:38])([CH3:37])[CH:31]=[C:30]2[CH3:39]

Participants

6

Reactant 4

HCID 63651,1-DichloroethaneHCID 7679Phenylacetyl chlorideHCID 6451240Aluminum(III) ChlorideHCID 58026756HCID 58026756, compound

Product 1

HCID 58026943HCID 58026943, compoundYield 82%

Reagents, catalysts & solvents 1

HCID 8857Ethyl AcetateSolvent

Conditions

Temperature
0 °C

Procedure

Aluminum chloride (97.0 mg, 0.73 mmol) was added to anhydrous dichloroethane (0.5 mL) and the solution was cooled to 0° C. Phenylacetyl chloride (97 μL, 0.73 mmol) and 6-(2-methoxyphenyl)-5-(4-methylbenzoyloxymethyl)-2,2,4-trimethyl-1,2-dihydroquinoline (Compound No. 13-3, 49.7 mg, 0.12 mmol) were added thereto and the reaction mixture was stirred at room temperature for 1.5 hours. Ethyl acetate (100 mL) was added to the reaction mixture, and the whole was washed with water (100 mL) and saturated brine (50 mL) successively, dried over anhydrous magnesium sulfate, and then the solvent was removed under reduced pressure. The residue was purified by silica gel column chromatography (hexane-ethyl acetate) to give the titled compound (53.6 mg) as a pale yellow amorphous product. (Yield 82%)

Workup

  1. addition13-3, 49.7 mg, 0.12 mmol) were added
  2. washthe whole was washed with water (100 mL) and saturated brine (50 mL) successively
  3. dry with materialdried over anhydrous magnesium sulfate
  4. customthe solvent was removed under reduced pressure
  5. customThe residue was purified by silica gel column chromatography (hexane-ethyl acetate)

Sources & evidence

ORD record
ord-53baff6a95734aa0b965d0d271e60910
Source dataset
uspto-grants-2013_04
Patent number
US08420635B2

Reaction notes

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