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Water → 4-Carboxymethoxy-3-ethoxyphenylboronic acid

HRID 30752
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인쇄 미리보기

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HRID 30752 반응식
[OH-].[Na+].[CH2:3]([O:5][C:6]1[CH:18]=[C:17]([B:19]2[O:23]C(C)(C)C(C)(C)[O:20]2)[CH:16]=[CH:15][C:7]=1[O:8][CH2:9][C:10]([O:12]CC)=[O:11])[CH3:4].O.C(OCC)(=O)C>C(O)C>[C:10]([CH2:9][O:8][C:7]1[CH:15]=[CH:16][C:17]([B:19]([OH:23])[OH:20])=[CH:18][C:6]=1[O:5][CH2:3][CH3:4])([OH:12])=[O:11]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 962WaterHCID 8857Ethyl AcetateHCID 14798Sodium HydroxideHCID 86605505HCID 86605505, 화합물

생성물 1

HCID 231342404-Carboxymethoxy-3-ethoxyphenylboronic acid수율 64.2%

시약·촉매·용매 1

HCID 702Ethanol용매

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온도
60 °C

실험 절차

A 2 mol/L aqueous solution of sodium hydroxide (2.14 mL) was added to a solution of ethyl [2-ethoxy-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenoxy]acetate (0.15 g) in ethanol (10 mL), and the resulting mixture was stirred at 60° C. for 3 hrs. Water and ethyl acetate were added to the reaction mixture. The aqueous layer was separated, washed with ethyl acetate, made acidic with the addition of 2 mol/L hydrochloric acid, and extracted with ethyl acetate. The organic layer was dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure to afford the title compound (0.066 g).

후처리

  1. customThe aqueous layer was separated
  2. washwashed with ethyl acetate
  3. additionmade acidic with the addition of 2 mol/L hydrochloric acid
  4. extractionextracted with ethyl acetate
  5. dry with materialThe organic layer was dried over anhydrous magnesium sulfate
  6. customThe solvent was evaporated under reduced pressure

출처 및 근거

ORD 기록
ord-9432fbf6457d43c09a8ad818b559f197
출처 데이터셋
uspto-grants-2008_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07423185B2

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