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Triisopropyl borate → HCID 46739418, 화합물

HRID 2403367
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HRID 2403367 반응식
Br[C:2]1[CH:3]=[N:4][CH:5]=[C:6]([O:8][CH2:9][C:10]2[CH:15]=[CH:14][C:13]([O:16][CH3:17])=[CH:12][CH:11]=2)[CH:7]=1.[B:18]([O:27][CH:28]([CH3:30])[CH3:29])([O:23][CH:24]([CH3:26])[CH3:25])OC(C)C.C([Li])CCC>C1COCC1>[CH3:17][O:16][C:13]1[CH:14]=[CH:15][C:10]([CH2:9][O:8][C:6]2[CH:5]=[N:4][CH:3]=[C:2]([B:18]3[O:23][C:24]([CH3:25])([CH3:26])[C:28]([CH3:29])([CH3:30])[O:27]3)[CH:7]=2)=[CH:11][CH:12]=1
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참가 물질

5

반응물 3

HCID 21531Triisopropyl borateHCID 226073453-Bromo-5-(4-methoxybenzyloxy)pyridineHCID 178418339Butyllithium

생성물 1

HCID 46739418HCID 46739418, 화합물

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

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온도
-78 °C

실험 절차

To a solution of 3-bromo-5-(4-methoxy-benzyloxy)-pyridine (300 mg) in THF (10 mL) was added triisopropyl borate (0.28 mL) and the mixture cooled to −78° C. Then n-butyllithium (0.49 mL of a 2.5 M solution in hexanes) was added maintaining the temperature below −65° C. The reaction mixture was then allowed to warm to −20° C. over 1 h and then quenched with 2 M aqueous hydrochloric acid (2 mL). The mixture was allowed to warm to room temperature over 1 h and then diluted with water (25 mL), the pH was adjusted to 7 and then extracted into ethyl acetate (3×25 mL). The combined organics were washed with brine (20 mL), dried (MgSO4) and reduced in vacuo. A mixture of the crude product and pinacol (236 mg) in toluene (15 mL) was then heated at reflux for 4 h. The mixture was then reduced in vacuo, dissolved in ethyl acetate (30 mL) and washed with water (2×30 mL) and brine (30 mL). The combined organics were dried (MgSO4) and reduced in vacuo to give 3-(4-methoxy-benzyloxy)-5-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-pyridine as an off-white solid (162 mg).

후처리

  1. temperaturemaintaining the temperature below −65° C
  2. temperatureto warm to −20° C. over 1 h
  3. customquenched with 2 M aqueous hydrochloric acid (2 mL)
  4. temperatureto warm to room temperature over 1 h
  5. additiondiluted with water (25 mL)
  6. extractionextracted into ethyl acetate (3×25 mL)
  7. washThe combined organics were washed with brine (20 mL)
  8. dry with materialdried (MgSO4)
  9. additionA mixture of the crude product and pinacol (236 mg) in toluene (15 mL)
  10. temperaturewas then heated
  11. temperatureat reflux for 4 h
  12. dissolutiondissolved in ethyl acetate (30 mL)
  13. washwashed with water (2×30 mL) and brine (30 mL)
  14. dry with materialThe combined organics were dried (MgSO4)

출처 및 근거

ORD 기록
ord-5ef0781c0bd745ae8fe044cb87b87902
출처 데이터셋
uspto-grants-2014_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08802670B2

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