Hydrochloric Acid → HCID 20082008, 화합물

HRID 1609589노트

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HRID 1609589 반응식
[Cl:1][C:2]1[CH:21]=[CH:20][C:5]([C:6]([C:8]2[CH:9]=[C:10]([C:17]([OH:19])=[O:18])[C:11](=[CH:15][CH:16]=2)[C:12]([OH:14])=[O:13])=[O:7])=[CH:4][CH:3]=1.CCOCC.[Cl:27][C:28]1[CH:33]=[CH:32][C:31]([Mg]Br)=[CH:30][CH:29]=1.Cl>O1CCCC1.C(OCC)(=O)C>[OH:7][C:6]([C:31]1[CH:32]=[CH:33][C:28]([Cl:27])=[CH:29][CH:30]=1)([C:5]1[CH:4]=[CH:3][C:2]([Cl:1])=[CH:21][CH:20]=1)[C:8]1[CH:9]=[C:10]([C:17]([OH:19])=[O:18])[C:11](=[CH:15][CH:16]=1)[C:12]([OH:14])=[O:13]

참가 물질

7

반응물 4

HCID 313Hydrochloric AcidHCID 3283Diethyl EtherHCID 200819974-(4-Chlorobenzoyl)phthalic acidHCID 178478191HCID 178478191, 화합물

생성물 1

HCID 20082008HCID 20082008, 화합물

시약·촉매·용매 2

HCID 8028Tetrahydrofuran용매HCID 8857Ethyl Acetate용매

실험 절차

To a solution of 2.00 g of 4-(4-chlorobenzoyl) phthalic acid in 63 ml of tetrahydrofuran was dropwise added 50 ml of ether solution (0.59M) of 4-chlorophenylmagnesium bromide at room temperature in 20 minutes. The reaction mixture was refluxed under heating for 3 hours, cooled with ice, hydrolyzed with 10% hydrochloric acid and shaken with ethyl acetate. The organic layer was washed with water, dried over anhydrous magnesium sulfate and concentrated in vacuo. The resultant residue was chromatographed on a column of silica gel, eluting with chloroform and methanol (2:1) to give crude 4-[hydroxybis(4-chlorophenyl)methyl]phthalic acid. This intermediate was provided for the following reaction without further purification.

후처리

  1. customat room temperature
  2. customin 20 minutes
  3. temperatureThe reaction mixture was refluxed
  4. temperatureunder heating for 3 hours
  5. washThe organic layer was washed with water
  6. dry with materialdried over anhydrous magnesium sulfate
  7. concentrationconcentrated in vacuo
  8. customThe resultant residue was chromatographed on a column of silica gel
  9. washeluting with chloroform and methanol (2:1)

출처 및 근거

ORD 기록
ord-83ea7f3567fa4ca088e2dcb6fb633f30
출처 데이터셋
uspto-grants-1995_03
특허 번호
US05401756

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