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Hydrochloric Acid → {4-[3,3-Bis-(4-bromo-phenyl)-2-ethoxy-allylsulfanyl]-2-methyl-phenoxy}-acetic Acid

HRID 1247678
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HRID 1247678 반응식
C[O:2][C:3](=[O:34])[CH2:4][O:5][C:6]1[CH:11]=[CH:10][C:9]([S:12][CH2:13][C:14]([O:30][CH2:31][CH3:32])=[C:15]([C:23]2[CH:28]=[CH:27][C:26]([Br:29])=[CH:25][CH:24]=2)[C:16]2[CH:21]=[CH:20][C:19]([Br:22])=[CH:18][CH:17]=2)=[CH:8][C:7]=1[CH3:33].[OH-].[Na+].Cl>C(O)C>[Br:29][C:26]1[CH:25]=[CH:24][C:23]([C:15]([C:16]2[CH:21]=[CH:20][C:19]([Br:22])=[CH:18][CH:17]=2)=[C:14]([O:30][CH2:31][CH3:32])[CH2:13][S:12][C:9]2[CH:10]=[CH:11][C:6]([O:5][CH2:4][C:3]([OH:34])=[O:2])=[C:7]([CH3:33])[CH:8]=2)=[CH:28][CH:27]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 313Hydrochloric AcidHCID 14798Sodium HydroxideHCID 10416238{4-[3,3-Bis-(4-bromo-phenyl)-2-ethoxy-allylsulfanyl]-2-methyl-phenoxy}-acetic acid methyl ester

생성물 1

HCID 10348426{4-[3,3-Bis-(4-bromo-phenyl)-2-ethoxy-allylsulfanyl]-2-methyl-phenoxy}-acetic Acid

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

{4-[3,3-Bis-(4-bromo-phenyl)-2-ethoxy-allylsulfanyl]-2-methyl-phenoxy}-acetic acid methyl ester (170 mg, 0.3 mmol, example 25) was dissolved in ethanol (5 ml). 1N NaOH (3 ml, 3 mmol) was added at room temperature and the reaction mixture was stirred for 30 min at room temperature, after which it was treated with 1N HCl (15 ml) and extracted with ethyl acetate (2×20 ml). The combined organic phases were dried and evaporated to give the title compound in 150 mg (90%) yield.

후처리

  1. extractionextracted with ethyl acetate (2×20 ml)
  2. customThe combined organic phases were dried
  3. customevaporated

출처 및 근거

ORD 기록
ord-38a66c32d58746c39c91bafc074fcc44
출처 데이터셋
uspto-grants-2006_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07129268B2

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