4-Bromobenzoyl chloride → (4-Bromo-phenyl)-(2-butyl-benzofuran-3-yl)-methanone

HRID 900367

반응식

HRID 900367 반응식
[CH2:1]([C:5]1[O:6][C:7]2[CH:13]=[CH:12][CH:11]=[CH:10][C:8]=2[CH:9]=1)[CH2:2][CH2:3][CH3:4].[Br:14][C:15]1[CH:23]=[CH:22][C:18]([C:19](Cl)=[O:20])=[CH:17][CH:16]=1.[Al+3].[Cl-].[Cl-].[Cl-]>ClCCl>[Br:14][C:15]1[CH:23]=[CH:22][C:18]([C:19]([C:9]2[C:8]3[CH:10]=[CH:11][CH:12]=[CH:13][C:7]=3[O:6][C:5]=2[CH2:1][CH2:2][CH2:3][CH3:4])=[O:20])=[CH:17][CH:16]=1

참가 물질

5

반응물 3

HCID 685154-Bromobenzoyl chlorideHCID 779512-ButylbenzofuranHCID 6451240Aluminum(III) Chloride

생성물 1

HCID 59655974(4-Bromo-phenyl)-(2-butyl-benzofuran-3-yl)-methanone수율 36%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

A solution of 2-n-butylbenzofurane (19.8 g, 114 mmol) and 4-bromobenzoyl chloride (25.0 g, 114 mmol) in dry dichloromethane (300 mL, 0.4 M) was cooled to 0° C. and treated with AlCl3 (16.6 g, 1.1 equiv., 125.4 mmol) in 3 portions. After the additions were complete, the solution was stirred for 3 h and carefully added to ice water. After separation, the aqueous layer was extracted with dichloromethane (2×200 mL) and the combined organic layers were washed with water, sat'd aq NaCl, dried over anhydrous MgSO4, filtered and concentrated in vacuo. Purification by flash column chromatography (1-2% ethyl acetate in heptane) afforded (4-bromo-phenyl)-(2-butyl-benzofuran-3-yl)-methanone (14.6 g, 36%).

후처리

  1. customAfter separation
  2. extractionthe aqueous layer was extracted with dichloromethane (2×200 mL)
  3. washthe combined organic layers were washed with water
  4. dry with materialdried over anhydrous MgSO4
  5. filtrationfiltered
  6. concentrationconcentrated in vacuo
  7. customPurification by flash column chromatography (1-2% ethyl acetate in heptane)

출처 및 근거

ORD 기록
ord-7b7e41567f2b4f37b192ea9201092184
출처 데이터셋
uspto-grants-2008_04
특허 번호
US07358248B2

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