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Potassium;tri(butan-2-yl)boranuide → HCID 10348167、化合物

HRID 357274
ノート
印刷プレビュー

反応式

HRID 357274 の反応式
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]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 4304157Potassium;tri(butan-2-yl)boranuide2 回HCID 10460748HCID 10460748、化合物

生成物 1

HCID 10348167HCID 10348167、化合物収率 94%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒2 回

反応条件

温度
500 °C

実験手順

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.

後処理

  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)

出典と根拠

ORDレコード
ord-0bd7304d63c347c99ac2bfc9a0cd9acc
出典データセット
uspto-grants-1998_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05840740

反応ノート

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このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート