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Sodium Methoxide → HCID 15220195, 화합물

HRID 583043
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HRID 583043 반응식
[CH3:1][O-:2].[Na+].Br[CH2:5][C:6]1[CH:7]=[C:8]([C:13]2[C:17]([Cl:18])=[C:16]([O:19][CH:20]([F:22])[F:21])[N:15]([CH3:23])[N:14]=2)[CH:9]=[CH:10][C:11]=1[Cl:12]>CO>[Cl:18][C:17]1[C:13]([C:8]2[CH:9]=[CH:10][C:11]([Cl:12])=[C:6]([CH2:5][O:2][CH3:1])[CH:7]=2)=[N:14][N:15]([CH3:23])[C:16]=1[O:19][CH:20]([F:22])[F:21]
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참가 물질

4

반응물 2

HCID 10942334Sodium MethoxideHCID 15220187HCID 15220187, 화합물

생성물 1

HCID 15220195HCID 15220195, 화합물

시약·촉매·용매 1

HCID 887Methanol용매2회

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온도
40 °C

실험 절차

1.6 g (9.0 mmol) of a 30% strength by weight solution of sodium methylate in methanol was added dropwise to a solution of 2.3 g (6.0 mmol) of 3-(3-bromomethyl-4-chlorophenyl)-4-chloro-5-difluoromethoxy-1-methyl-1H-pyrazole in 60 ml of methanol. The reaction mixture was stirred at 40° C. for 3 hours and then concentrated. The residue was taken up in water and dichloromethane, after which concentrated hydrochloric acid was added until the acid reaction took place. Product remaining in the aqueous phase was extracted with dichloromethane. The combined dichloromethane phases were dried over magnesium sulfate and concentrated. Yield: 1.8 g.

후처리

  1. concentrationconcentrated
  2. additiondichloromethane, after which concentrated hydrochloric acid was added until the acid reaction
  3. extractionwas extracted with dichloromethane
  4. dry with materialThe combined dichloromethane phases were dried over magnesium sulfate
  5. concentrationconcentrated

출처 및 근거

ORD 기록
ord-de13c18d1b0b49758baef40876695db0
출처 데이터셋
uspto-grants-1999_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05928999

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