Tetrahydrofuran → 1,6-Heptadiene-3,5-diol

HRID 1485835

反応式

HRID 1485835 の反応式
[I-].C[S+](C)C.[CH2:6]([Li])[CH2:7][CH2:8][CH3:9].[O:11]1C[CH:12]1[CH2:14][CH2:15]C1CO1.[NH4+].[Cl-].C1C[O:24]CC1>>[CH2:9]=[CH:8][CH:7]([OH:24])[CH2:6][CH:12]([OH:11])[CH:14]=[CH2:15]

参加物

6

反応条件

温度
-10 °C

実験手順

To a stirred solution of tri-methylsulfonium iodide (6.12 g, 30 mmol) in dry THF (50 mL) at −10° C. was added drop-wise butyllithium (14 mL, 2.5 M in hexane). The reaction mixture was stirred at −10° C. for 30 min, and a solution of diepoxide 32 (570 mg, 5 mmol) in dry THF (5 mL) was added. The reaction mixture was allowed to warm to room temperature, and the white suspension was stirred overnight. The mixture was treated with a saturated aqueous NH4Cl solution (15 mL), extracted with CH2Cl2 (3×10 mL), dried over Na2SO4, and concentrated. The crude product was purified on silica gel (pentane/ether 50/50) to yield the compound 33 (360 mg, 45% yield)

後処理

  1. temperatureto warm to room temperature
  2. stirringthe white suspension was stirred overnight
  3. extractionextracted with CH2Cl2 (3×10 mL)
  4. dry with materialdried over Na2SO4
  5. concentrationconcentrated
  6. customThe crude product was purified on silica gel (pentane/ether 50/50)

出典と根拠

ORDレコード
ord-bc9c99fa78cb4ff296590cc7da773db6
出典データセット
uspto-grants-2016_08
特許番号
US09422320B2

関連ノート

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