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Potassium Carbonate → 2-(Chloromethyl)-5-(3,4-dichlorophenyl)-1,3,4-oxadiazole

HRID 334523
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반응식

HRID 334523 반응식
[Cl:1][C:2]1[CH:3]=[C:4]([CH:13]=[CH:14][C:15]=1[Cl:16])[C:5]([NH:7][NH:8][C:9](=[O:12])[CH2:10][Cl:11])=O.C([O-])([O-])=O.[K+].[K+]>CC(C)=O>[Cl:11][CH2:10][C:9]1[O:12][C:5]([C:4]2[CH:13]=[CH:14][C:15]([Cl:16])=[C:2]([Cl:1])[CH:3]=2)=[N:7][N:8]=1
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참가 물질

4

반응물 2

HCID 11430Potassium CarbonateHCID 674793863,4-dichloro-N'-(2-chloroacetyl)benzohydrazide

생성물 1

HCID 27634662-(Chloromethyl)-5-(3,4-dichlorophenyl)-1,3,4-oxadiazole수율 40%

시약·촉매·용매 1

HCID 180Acetone용매

실험 절차

A mixture of compound 9 (120 mg, 0.263 mmol), compound A (76 mg, 0.263 mmol) and K2CO3 (72.58 mg, 0.526 mmol) was heated under reflux in 25 ml of acetone for 3 hours. The reaction mixture was cooled to ambient temperature, filtered and the filtrate was evaporated to obtain crude residue which was purified by column chromatography using MeOH/DCM (15:85) as an eluent to obtain compound 10 as a yellow colored gummy material (75 mg). Yield: 40%.

후처리

  1. temperaturewas heated
  2. filtrationfiltered
  3. customthe filtrate was evaporated
  4. customto obtain crude residue which
  5. customwas purified by column chromatography

출처 및 근거

ORD 기록
ord-4e977790c0954e7b97e3a60e8940066d
출처 데이터셋
uspto-grants-2014_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08883827B2

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