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1,4-Dioxaspiro[4.5]decan-8-one → 8-Benzyl-1,4-dioxaspiro[4.5]decan-8-ol

HRID 1795853
ノート
印刷プレビュー

反応式

HRID 1795853 の反応式
[CH2:1]([Mg]Cl)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[CH2:10]1[O:20][C:13]2([CH2:18][CH2:17][C:16](=[O:19])[CH2:15][CH2:14]2)[O:12][CH2:11]1>C1COCC1>[CH2:1]([C:16]1([OH:19])[CH2:17][CH2:18][C:13]2([O:20][CH2:10][CH2:11][O:12]2)[CH2:14][CH2:15]1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1
参加物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 5674151,4-Dioxaspiro[4.5]decan-8-oneHCID 178418336HCID 178418336、化合物

生成物 1

HCID 221798308-Benzyl-1,4-dioxaspiro[4.5]decan-8-ol収率 81%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒2 回

実験手順

A 0° C. solution of 2M benzylmagnesium chloride in THF (20 mL) was treated with a solution of 1,4-cyclohexanedione mono-ethylene ketal (6.24 g, 40 mmol) in THF (50 mL), warmed to room temperature, stirred overnight, quenched with saturated NH4Cl (100 mL), and extracted with ethyl acetate (3×100 mL). The combined extracts were washed with water and brine, dried (Na2SO4), filtered, and concentrated. The concentrate was purified by flash column chromatography on silica gel with 6:1 hexanes/ethyl acetate to provide the desired product (8.08 g, 81%). MS (CI) m/e 231(M−18)+, 249 (M+H) +, 266.2 (M+18)+.

後処理

  1. customquenched with saturated NH4Cl (100 mL)
  2. extractionextracted with ethyl acetate (3×100 mL)
  3. washThe combined extracts were washed with water and brine
  4. dry with materialdried (Na2SO4)
  5. filtrationfiltered
  6. concentrationconcentrated
  7. customThe concentrate was purified by flash column chromatography on silica gel with 6:1 hexanes/ethyl acetate

出典と根拠

ORDレコード
ord-43b4c56d3f2448b0bbc3832a9f9e98a5
出典データセット
uspto-grants-2006_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07030115B2

反応ノート

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