Sulfuric Acid → HCID 12480958、化合物

HRID 1854228ノート

反応式

HRID 1854228 の反応式
C[O:2][CH:3](OC)[CH2:4][O:5][CH:6]1[CH2:11][CH2:10][CH2:9][CH2:8][CH2:7]1.S(=O)(=O)(O)O>O>[CH:6]1([O:5][CH2:4][CH:3]=[O:2])[CH2:11][CH2:10][CH2:9][CH2:8][CH2:7]1

参加物

4

反応条件

温度
100 °C

実験手順

Acidify a mixture of (2,2-dimethoxyethoxy)cyclohexane and water (30 mL) to a pH of 1.0 with sulfuric acid (9.0 M aqueous solution), and connect the mixture to a short-path distillation head. Reduce the pressure to 26.7 kPa and heat the mixture to 100° C. for 1 h. Cool the mixture to room temperature, then extract the aqueous layer with TBME (2×75 mL). Wash the combined organic layers with saturated aqueous NaHCO3 (75 mL) and saturated aqueous NaCl (75 mL). Dry the organic phase over MgSO4, filter, and concentrate the filtrate under reduced pressure to furnish the title compound (634 mg, 51% yield). 1H NMR (400 MHz, CDCl3): δ 9.73 (t, J=1.0 Hz, 1H), 4.06 (d, J=1.0 Hz, 2H), 3.31 (tt, J=9.2, 3.9 Hz, 1H), 1.95-1.89 (m, 2H), 1.79-1.68 (m, 2H), 1.57-1.50 (m, 1H), 1.39-1.20 (m, 5H).

後処理

  1. temperatureCool the mixture to room temperature
  2. extractionextract the aqueous layer with TBME (2×75 mL)
  3. washWash the combined organic layers with saturated aqueous NaHCO3 (75 mL) and saturated aqueous NaCl (75 mL)
  4. dry with materialDry the organic phase over MgSO4
  5. filtrationfilter
  6. concentrationconcentrate the filtrate under reduced pressure

出典と根拠

ORDレコード
ord-0eb91556c55245a7a5c8526656c11fa4
出典データセット
uspto-grants-2015_02
特許番号
US08962659B2

反応ノート

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