2-Phenylethyl Acetate → 4-(5-Bromo-2-chlorobenzoyl)phenethyl acetate

HRID 425057노트

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HRID 425057 반응식
[Br:1][C:2]1[CH:3]=[CH:4][C:5]([Cl:11])=[C:6]([CH:10]=1)[C:7]([OH:9])=O.C(Cl)(=O)C(Cl)=O.[Cl-].[Cl-].[Cl-].[Al+3].[C:22]([O:25][CH2:26][CH2:27][C:28]1[CH:33]=[CH:32][CH:31]=[CH:30][CH:29]=1)(=[O:24])[CH3:23]>C(Cl)Cl.CN(C=O)C>[C:22]([O:25][CH2:26][CH2:27][C:28]1[CH:33]=[CH:32][C:31]([C:7](=[O:9])[C:6]2[CH:10]=[C:2]([Br:1])[CH:3]=[CH:4][C:5]=2[Cl:11])=[CH:30][CH:29]=1)(=[O:24])[CH3:23]

참가 물질

7

실험 절차

To a solution of commercially available 5-bromo-2-chlorobenzoic acid (5 g, 21.23 mmol) in 30 mL of anhydrous DCM was added a catalytic amount of DMF followed by oxalyl chloride (1.95 mL, 22.3 mmol) and stirred for 2 h at room temperature. A mixture of aluminum trichloride (3.68 g, 27.6 mmol) and phenethyl acetate (3.38 mL, 21.23 mmol) in 15 mL DCM was cooled in an ice-bath and the acid chloride was transferred to it using a canula. The mixture was stirred at room temperature for 4 h. The mixture was poured into 100 mL of ice-cold water and the organic layer was isolated. The aqueous solution was extracted with 25 mL DCM. The combined organic solution was washed with brine (25 mL) and dried (Na2SO4), filtered and evaporated. Purification on silica gel using an ISCO column with 5:1 hexane:EtOAc followed by 10:1 hexane:EtOAc gave intermediate BF (2.1 g, yield 26%). 1H NMR (300 MHz, CDCl3): δ 8.12 (d, J=2.4 Hz, 1H), 7.71 (d, J=8.4 Hz, 1H), 7.59 (d, J=2.7 Hz, 1H), 7.56 (d, J=8.4 Hz, 1H), 7.36 (s, 1H), 7.33 (d, J=8.4 Hz, 1H), 7.30 (d, J=8.4 Hz, 1H), 4.31 (t, J=6.9, 6.6 Hz, 2H), 3.01 (t, J=6.9, 6.6 Hz, 2H), 2.04 (s, 3H).

후처리

  1. temperaturewas cooled in an ice-bath
  2. stirringThe mixture was stirred at room temperature for 4 h
  3. customthe organic layer was isolated
  4. extractionThe aqueous solution was extracted with 25 mL DCM
  5. washThe combined organic solution was washed with brine (25 mL)
  6. dry with materialdried (Na2SO4)
  7. filtrationfiltered
  8. customevaporated
  9. customPurification on silica gel using an ISCO column with 5:1 hexane
  10. customEtOAc gave intermediate BF (2.1 g, yield 26%)

출처 및 근거

ORD 기록
ord-9ace20d09e36429da144d73d2a957246
출처 데이터셋
uspto-grants-2012_01
특허 번호
US08106021B2

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