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Hydrochloric Acid → HCID 18448299, 화합물

HRID 1269692
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HRID 1269692 반응식
[CH2:1]([N:5]([CH2:20][C:21]1[CH:33]=[CH:32][C:24]([O:25][CH2:26][C:27]([O:29]CC)=[O:28])=[C:23]([CH3:34])[CH:22]=1)[C:6]1[C:7]([CH3:19])=[C:8]([C:12]2[CH:17]=[CH:16][C:15]([CH3:18])=[CH:14][CH:13]=2)[CH:9]=[CH:10][CH:11]=1)[CH2:2][CH2:3][CH3:4].[OH-].[Na+].Cl>C1COCC1.O>[CH2:1]([N:5]([CH2:20][C:21]1[CH:33]=[CH:32][C:24]([O:25][CH2:26][C:27]([OH:29])=[O:28])=[C:23]([CH3:34])[CH:22]=1)[C:6]1[C:7]([CH3:19])=[C:8]([C:12]2[CH:17]=[CH:16][C:15]([CH3:18])=[CH:14][CH:13]=2)[CH:9]=[CH:10][CH:11]=1)[CH2:2][CH2:3][CH3:4]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

HCID 313Hydrochloric AcidHCID 14798Sodium HydroxideHCID 58622877HCID 58622877, 화합물

생성물 1

HCID 18448299HCID 18448299, 화합물수율 93.2%

시약·촉매·용매 2

HCID 962Water용매2회HCID 8028Tetrahydrofuran용매

실험 절차

Ethyl (4-{[butyl(2,4′-dimethyl-1,1′-biphenyl-3-yl)amino]methyl}-2-methylphenoxy)acetate (12.7 g, 27.6 mmol) was dissolved in THF (210 mL) and water (70 ml) was added, followed by 2M aq. NaOH (61 mL, 122 mmol). The reaction was stirred at room temperature for 1/2 hr and then evaporated to give a white slurry. The suspension was diluted with water (100 mL) and pH adjusted to pH7 with 2M aq HCl. EtOAc (200 mL) the aqueous layer was separated and extracted with EtOAc (2×100 mL). The combined organics were washed with brine (200 mL), dried (Na2SO4) and concentrated In vacuo to give the title compound as a white foam (11.1 g).

후처리

  1. customevaporated
  2. customto give a white slurry
  3. customEtOAc (200 mL) the aqueous layer was separated
  4. extractionextracted with EtOAc (2×100 mL)
  5. washThe combined organics were washed with brine (200 mL)
  6. dry with materialdried (Na2SO4)
  7. concentrationconcentrated In vacuo

출처 및 근거

ORD 기록
ord-0897a9c66f724b238cde263b17e68c31
출처 데이터셋
uspto-grants-2007_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07199239B2

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