Mandelic Acid → HCID 12390395、化合物

HRID 82263

反応式

HRID 82263 の反応式
[OH:1][CH:2]([C:6]1[CH:11]=[CH:10][CH:9]=[CH:8][CH:7]=1)[C:3]([OH:5])=[O:4].CC1C=CC(S(O)(=O)=O)=CC=1.[O:23]1[CH:28]=[CH:27][CH2:26][CH2:25][CH2:24]1>C(Cl)Cl>[C:6]1([CH:2]([O:1][CH:24]2[CH2:25][CH2:26][CH2:27][CH2:28][O:23]2)[C:3]([OH:5])=[O:4])[CH:11]=[CH:10][CH:9]=[CH:8][CH:7]=1

参加物

5

反応条件

温度
0 °C

実験手順

To a stirred solution of hydroxy-phenyl-acetic acid (2 g, 13.4 mmol) in DCM (30 mL) was added PTSA (51.2 mg, 0.27 mmol) at 0° C. followed by the addition of 3,4-dihydro-2H-pyran (1.55 g, 18.4 mmol). The mixture was stirred at 0° C. for another 15 min and then gradually warmed up to room temperature and stirred for a further 1.5 hours. The reaction mixture was diluted with DCM (100 mL). The organic phase was washed with saturated aq. Na2CO3 (2×20 mL), water (20 mL), brine (20 mL), dried (Na2SO4) and evaporated in vacuo. The crude material was purified by column chromatography on silica gel (EtOAc:petroleum ether 2:5) to afford the title compound as a yellow sticky solid in 48% yield, 1.5 g. LCMS (system 10): Rt=1.82 min; m/z 237 [M+H]+.

後処理

  1. temperaturegradually warmed up to room temperature
  2. stirringstirred for a further 1.5 hours
  3. washThe organic phase was washed with saturated aq. Na2CO3 (2×20 mL), water (20 mL), brine (20 mL)
  4. dry with materialdried (Na2SO4)
  5. customevaporated in vacuo
  6. customThe crude material was purified by column chromatography on silica gel (EtOAc:petroleum ether 2:5)

出典と根拠

ORDレコード
ord-a1c255ddb94d4dabba7c7773e72b1649
出典データセット
uspto-grants-2014_09
特許番号
US08846698B2

関連ノート

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