Delta-Valerolactone → 2-phenyltetrahydro-2H-pyran-2-ol

HRID 714257

反応式

HRID 714257 の反応式
[C:1]1(=[O:7])[O:6][CH2:5][CH2:4][CH2:3][CH2:2]1.[C:8]1([Mg]Br)[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=1>C1COCC1>[C:8]1([C:1]2([OH:7])[CH2:2][CH2:3][CH2:4][CH2:5][O:6]2)[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=1

参加物

4

反応物 2

HCID 10953Delta-ValerolactoneHCID 178418255HCID 178418255、化合物

生成物 1

HCID 145879022-phenyltetrahydro-2H-pyran-2-ol収率 55.3%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

実験手順

To a solution of delta-valerolactone (1.854 mL, 19.98 mmol) in THF (20 mL) was added 1M phenylmagnesium bromide (19.98 mL, 19.98 mmol) dropwise at room temperature (exothermic), and the mixture was stirred at room temperature for 5 hrs. Then the reaction was quenched with saturated NH4Cl and extracted with EtOAc. The extract was washed with brine, and the combined aqueous layers were back extracted with EtOAc once and combined. The extracts were dried over Na2SO4 and evaporated to give an oily residue. It was purified by Combiflash (120 g silica gel) eluting with 4:6 followed by 1:1 EtOAc-hexane to give 1.97 g of 2-phenyltetrahydro-2H-pyran-2-ol as oil.

後処理

  1. customThen the reaction was quenched with saturated NH4Cl
  2. extractionextracted with EtOAc
  3. washThe extract was washed with brine
  4. extractionthe combined aqueous layers were back extracted with EtOAc once
  5. dry with materialThe extracts were dried over Na2SO4
  6. customevaporated
  7. customto give an oily residue
  8. customIt was purified by Combiflash (120 g silica gel)
  9. washeluting with 4:6

出典と根拠

ORDレコード
ord-91872494061745a6a58c5f3c89753e31
出典データセット
uspto-grants-2015_11
特許番号
US09187437B2

関連ノート

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