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Water → 2-(4-Bromo-phenyl)-[1,3]dioxolane-2-carboxylic Acid

HRID 1697624
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HRID 1697624 반응식
C([O:3][C:4]([C:6]1([C:11]2[CH:16]=[CH:15][C:14]([Br:17])=[CH:13][CH:12]=2)[O:10][CH2:9][CH2:8][O:7]1)=[O:5])C.O.[OH-].[Li+]>O1CCCC1>[Br:17][C:14]1[CH:13]=[CH:12][C:11]([C:6]2([C:4]([OH:5])=[O:3])[O:7][CH2:8][CH2:9][O:10]2)=[CH:16][CH:15]=1
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참가 물질

5

반응물 3

HCID 962WaterHCID 3939Lithium HydroxideHCID 667720462-(4-Bromo-phenyl)-[1,3]dioxolane-2-carboxylic Acid Ethyl Ester

생성물 1

HCID 667718452-(4-Bromo-phenyl)-[1,3]dioxolane-2-carboxylic Acid수율 66%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

To a solution of 2-(4-Bromo-phenyl)-[1,3]dioxolane-2-carboxylic acid ethyl ester (example 346a), 300 mg) in tetrahydrofuran (2 mL) and water (2 mL) was added lithium hydroxide (41 mg) in two portions. The reaction mixture was stirred at room temperature over 2 days then concentrated in vacuo. The residue was acidified to pH=1 with aqueous hydrochloric acid solution (0.1N) extracted with ethyl acetate. The combined organic layer were washed with brine, dried over sodium sulfate, filtered and evaporated in vacuo to yield the title compound as a colorless oil (225 mg; 66%). MS (ESI): m/z=271.1 [M−H]−.

후처리

  1. concentrationthen concentrated in vacuo
  2. extractionextracted with ethyl acetate
  3. washThe combined organic layer were washed with brine
  4. dry with materialdried over sodium sulfate
  5. filtrationfiltered
  6. customevaporated in vacuo

출처 및 근거

ORD 기록
ord-f52f5cd273d54a36960122ffd9866e34
출처 데이터셋
uspto-grants-2012_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08163793B2

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