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Hydrochloric Acid → 1-(4-Bromo-2-fluorophenyl)-2-chloroethanone

HRID 2403328
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HRID 2403328 반응식
[Br:1][C:2]1[CH:10]=[CH:9][C:5]([C:6](Cl)=[O:7])=[C:4]([F:11])[CH:3]=1.C[Si](C=[N+]=[N-])(C)C.Cl.BrCC(C1C=CC(Br)=C(F)C=1)=O.[Cl:32][CH2:33]C(C1C=CC(Br)=C(F)C=1)=O>C(#N)C.C1COCC1.CCOC(C)=O>[Br:1][C:2]1[CH:10]=[CH:9][C:5]([C:6](=[O:7])[CH2:33][Cl:32])=[C:4]([F:11])[CH:3]=1
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참가 물질

9

반응물 5

HCID 313Hydrochloric AcidHCID 167693TrimethylsilyldiazomethaneHCID 27340264-Bromo-2-fluorobenzoyl chlorideHCID 533503281-(4-Bromo-3-fluorophenyl)-2-chloroethan-1-oneHCID 534166144-Bromo-3-fluorophenacyl bromide

생성물 1

HCID 790149471-(4-Bromo-2-fluorophenyl)-2-chloroethanone

시약·촉매·용매

3
HCID 6342Acetonitrile용매HCID 8028Tetrahydrofuran용매HCID 8857Ethyl Acetate용매

실험 절차

To a stirred solution of 4-bromo-2-fluorobenzoyl chloride (33 g, CAS 151982-51-3) in acetonitrile (150 ml) and THF (150 ml) at 0-5° C. was added dropwise (trimethylsilyl)diazomethane (83.4 ml, 2 M solution in hexane). The reaction mixture was stirred at room temperature for 30 min. TLC analysis showed the reaction was complete. 37% Hydrochloric acid (23.2 ml) was then added dropwise at 0-5° C. and the reaction mixture was stirred at room temperature for 1 hour. The reaction mixture was then poured into EtOAc and extracted sequentially with aq. Na2CO3 solution, water and saturated brine. The organic layer was then dried over Na2SO4 and concentrated in vacuo to afford a ca 1:1 mixture of 2-bromo-1-(4-bromo-3-fluoro-phenyl)-ethanone and 2-chloro-1-(4-bromo-3-fluoro-phenyl)-ethanone (34.4 g, 98%) as a yellow solid which was used in the next step without further purification. MS (EI): 203 ([{81Br}M-CH2Cl]+, 201 ([{79Br}M-CH2Cl]+).

후처리

  1. stirringthe reaction mixture was stirred at room temperature for 1 hour
  2. extractionextracted sequentially with aq. Na2CO3 solution, water and saturated brine
  3. dry with materialThe organic layer was then dried over Na2SO4
  4. concentrationconcentrated in vacuo
  5. customto afford a ca
  6. customwas used in the next step without further purification

출처 및 근거

ORD 기록
ord-ab87fd07f31a4eee9b58ae88dc40cf9f
출처 데이터셋
uspto-grants-2014_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08802673B2

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