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Hydrochloric Acid → 1H-Indol-2-ylboronic acid

HRID 1486660
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HRID 1486660 반응식
[NH:1]1[C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[CH:3]=[CH:2]1.[Li]CCCC.[B:15](OC(C)C)([O:20]C(C)C)[O:16]C(C)C.Cl.C([O-])(O)=O.[Na+]>C1COCC1>[NH:1]1[C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[CH:3]=[C:2]1[B:15]([OH:20])[OH:16]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 5

HCID 313Hydrochloric AcidHCID 798IndoleHCID 21531Triisopropyl borateHCID 516892Sodium BicarbonateHCID 178418339Butyllithium

생성물 1

HCID 225673581H-Indol-2-ylboronic acid수율 31.1%

시약·촉매·용매 1

HCID 8028
Tetrahydrofuran
용매

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온도
-40 °C

실험 절차

To the SEM-protected indole prepared in step 1 (0.99 g, 4.0 mmol) in THF (10 mL) at −40° C. was added n-BuLi (2.5 M in hexanes, 1.9 mL, 4.8 mmol). The mixture was stirred at −40° C. for 1 h and then triisopropyl borate (1.2 mL, 5.2 mmol) was added. The mixture was allowed to warm to room temperature while stirring for 18 h. To the reaction mixture was added 1N HCl (aq). The mixture was stirred at room temperature for 30 minutes. The mixture was then adjusted to pH˜5 using saturated NaHCO3 (aq) The mixture was extracted with ether. The combined ether extracts were washed with water and brine, dried (Na2SO4), filtered, and concentrated in vacuo. The residue was purified by silica gel chromatography (0-50% EtOAc/hex over 30 minutes) to provide the indole boronic acid (0.20 g, 17%).

후처리

  1. temperatureto warm to room temperature
  2. stirringwhile stirring for 18 h
  3. stirringThe mixture was stirred at room temperature for 30 minutes
  4. extractionwas extracted with ether
  5. washThe combined ether extracts were washed with water and brine
  6. dry with materialdried (Na2SO4)
  7. filtrationfiltered
  8. concentrationconcentrated in vacuo
  9. customThe residue was purified by silica gel chromatography (0-50% EtOAc/hex over 30 minutes)

출처 및 근거

ORD 기록
ord-b423dad14c8a494b8923030fff45628f
출처 데이터셋
uspto-grants-2016_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09428475B2

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