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Potassium;tri(butan-2-yl)boranuide → HCID 10348167, 화합물

HRID 357274
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HRID 357274 반응식
CCC(C)[BH-](C(C)CC)C(C)CC.[K+].[Si:15]([O:22][CH2:23][CH2:24][CH2:25][C@H:26]([C@@H:28]1[C@:45]2([CH3:46])[C@H:31]([C@H:32]3[C@H:42]([CH2:43][CH2:44]2)[C@:40]2([CH3:41])[C@H:35]([CH2:36][C@@H:37]([O:47][CH:48]4[CH2:53][CH2:52][CH2:51][CH2:50][O:49]4)[CH2:38][CH2:39]2)[CH2:34][C:33]3=[O:54])[CH2:30][CH2:29]1)[CH3:27])([C:18]([CH3:21])([CH3:20])[CH3:19])([CH3:17])[CH3:16]>C1COCC1>[Si:15]([O:22][CH2:23][CH2:24][CH2:25][C@H:26]([C@@H:28]1[C@:45]2([CH3:46])[C@H:31]([C@H:32]3[C@H:42]([CH2:43][CH2:44]2)[C@:40]2([CH3:41])[C@H:35]([CH2:36][C@@H:37]([O:47][CH:48]4[CH2:53][CH2:52][CH2:51][CH2:50][O:49]4)[CH2:38][CH2:39]2)[CH2:34][C@H:33]3[OH:54])[CH2:30][CH2:29]1)[CH3:27])([C:18]([CH3:19])([CH3:20])[CH3:21])([CH3:17])[CH3:16]
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참가 물질

4

반응물 2

HCID 4304157Potassium;tri(butan-2-yl)boranuide2회HCID 10460748HCID 10460748, 화합물

생성물 1

HCID 10348167HCID 10348167, 화합물수율 94%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매2회

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온도
500 °C

실험 절차

K-Selectride® (potassium tri-sec-butylborohydride) (8.9 ml, 1M in THF, 8.9 mmol) was added dropwise via syringe to a solution of ketone 2005 (1.7 g, 3.0 mmol) in dry THF (50 ml) at room temperature under argon. The reaction mixture was heated to 500° C. in an oil bath and stirred for 5 hours. The mixture was allowed to cool to room temperature and then quenched by adding 30% H2O2 dropwise until the evolution of gas ceased. Saturated aqueous NH4Cl solution was added and the aqueous solution was extracted (3×) with Et 20. The combined organic extracts were washed with aqueous saturated NaHCO3 solution (2×), distilled H2O (2×), and aqueous saturated NaCl solution, dried over anhydrous MgSO4, filtered, and the solvent was removed in vacuo. The crude product was purified by flash chromatography (SiO2, hexanes:EtOAc 10:1) giving alcohol 2006 as a white solid (1.6 g, 94%). 1H NMR (500 MHz, CDCl) δ 4.73-4.66 (m, 1 H, THP methine H), 3.95-3.85 (m, 1 H, THP CH2), 3.82 (s, 1 H, C-7 H), 3.66-3.52 (m, 3 H, THP CH2C & C-24 H), 3.50-3.45 (m, 1H, C-3 H), 1.08 (s, 3H, C-19 H), 0.91 (d, J=6.6 Hz, C-21 H), 0.89 (s, 9 H, t-Bu), 0.64 (s, 3 H, C-18 H), 0.04 (s, 6 H, TBDMS CH3); MS (CI/isobutane) m/z 577 (M+1, 5%), 493 (M+1-THP, 22%), 475 (M+1-THPOH, 26%), 458 (M+1-THPOH-H2O, 38%), 343 (M+1-THPOH-TBDMSOH, 80%), 325 (M+1-THPOH-TBDMSOH-H2O, 100%); IR (CHCl3) 3430, 2860 cm-1 ; m.p. 130°-133° C.; Anal. calcd. for C35H64 O4Si: C=72.86, H=11.18; Found: C=72.69, H=11.32.

후처리

  1. temperatureto cool to room temperature
  2. customquenched
  3. additionby adding 30% H2O2 dropwise until the evolution of gas
  4. additionSaturated aqueous NH4Cl solution was added
  5. extractionthe aqueous solution was extracted (3×) with Et 20
  6. washThe combined organic extracts were washed with aqueous saturated NaHCO3 solution (2×)
  7. distillationdistilled H2O (2×), and aqueous saturated NaCl solution
  8. dry with materialdried over anhydrous MgSO4
  9. filtrationfiltered
  10. customthe solvent was removed in vacuo
  11. customThe crude product was purified by flash chromatography (SiO2, hexanes:EtOAc 10:1)

출처 및 근거

ORD 기록
ord-0bd7304d63c347c99ac2bfc9a0cd9acc
출처 데이터셋
uspto-grants-1998_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05840740

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