1,1'-Carbonyldiimidazole → HCID 86697167, 화합물

HRID 237506

반응식

HRID 237506 반응식
[Br:1][C:2]1[C:14]([CH3:15])=[CH:13][C:5]([O:6][C:7]([CH3:12])([CH3:11])[C:8](O)=[O:9])=[CH:4][C:3]=1[CH3:16].C(N1C=CN=C1)([N:19]1C=CN=C1)=O.O.[OH-].[NH4+]>O1CCCC1>[Br:1][C:2]1[C:14]([CH3:15])=[CH:13][C:5]([O:6][C:7]([CH3:12])([CH3:11])[C:8]([NH2:19])=[O:9])=[CH:4][C:3]=1[CH3:16]

참가 물질

5

반응물 3

HCID 682631,1'-CarbonyldiimidazoleHCID 20990264HCID 20990264, 화합물HCID 86589665Water ammonium hydroxide

생성물 1

HCID 86697167HCID 86697167, 화합물

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

2-(4-Bromo-3,5-dimethyl-phenoxy)-2-methyl-propionic acid (500 mg) is dissolved in 10 mL of tetrahydrofurane, 1,1′-carbonyldimidazole (217 mg) and 30% ammonium hydroxide water solution are added and the reaction mixture is stirred at room temperature for 3 h. The reaction mixture is concentrated under vacuum, ethyl acetate is added and the organic solution is washed with a 10% HCl water solution. The organic phase is separated, dried over sodium sulfate and concentrated under vacuum to give the title compound. Yield: 300 mg.

후처리

  1. concentrationThe reaction mixture is concentrated under vacuum, ethyl acetate
  2. additionis added
  3. washthe organic solution is washed with a 10% HCl water solution
  4. customThe organic phase is separated
  5. dry with materialdried over sodium sulfate
  6. concentrationconcentrated under vacuum

출처 및 근거

ORD 기록
ord-f4abee1dccff4f1590921d1abbbdd41a
출처 데이터셋
uspto-grants-2014_02
특허 번호
US08642585B2

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