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Hydrochloric Acid → HCID 70815867, 화합물

HRID 1843016
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HRID 1843016 반응식
Br[C:2]1[CH:7]=[CH:6][C:5]([CH2:8][S:9]([CH3:12])(=[O:11])=[O:10])=[C:4]([F:13])[CH:3]=1.Cl[CH:15]([CH3:21])[C:16]([O:18][CH2:19][CH3:20])=[O:17].Cl>CN(C)C=O.FC(F)(F)C(O)=O.[Mn]>[F:13][C:4]1[CH:3]=[C:2]([CH:15]([CH3:21])[C:16]([O:18][CH2:19][CH3:20])=[O:17])[CH:7]=[CH:6][C:5]=1[CH2:8][S:9]([CH3:12])(=[O:11])=[O:10]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 3

HCID 313Hydrochloric AcidHCID 10807Ethyl 2-chloropropionateHCID 27614484-Bromo-2-fluoro-1-(methylsulfonylmethyl)benzene

생성물 1

HCID 70815867HCID 70815867, 화합물수율 45%

시약·촉매·용매 3

HCID 6422Trifluoroacetic acid촉매HCID 23930Manganese
촉매
HCID 6228Dimethylformamide용매

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온도
60 °C

실험 절차

To a stirred solution of 4-bromo-2-fluoro-1-(methylsulfonylmethyl)benzene (2 g, 7.487 mmol) in dimethylformamide (11 mL) were added ethyl 2-chloropropionate (1.24 mL, 9.733 mmol), manganese (822 mg, 14.974 mmol) and (2,2′-bipyridine)nickel(II)-dibromide (196 mg, 0.524 mmol). Trifluoroacetic acid (4 drops) was added. The reaction mixture was stirred overnight at 60° C. After cooling down to room temperature, the mixture was hydrolyzed by 1N HCl (30 mL) and extracted with ethyl acetate (3×50 mL). The organic layer was dried over magnesium sulfate and filtered. The solvent was removed in vacuo. The crude product was purified by CC (eluent: ethyl acetate/cyclohexane (1:1)) to give ethyl 2-(3-fluoro-4-(methylsulfonylmethyl)phenyl)propanoate (966 mg, 45%).

후처리

  1. temperatureAfter cooling down to room temperature
  2. extractionextracted with ethyl acetate (3×50 mL)
  3. dry with materialThe organic layer was dried over magnesium sulfate
  4. filtrationfiltered
  5. customThe solvent was removed in vacuo
  6. customThe crude product was purified by CC (eluent: ethyl acetate/cyclohexane (1:1))

출처 및 근거

ORD 기록
ord-f86bb2dd99074558b701310666cac967
출처 데이터셋
uspto-grants-2015_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08946204B2

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