Cesium carbonate → 4-Methoxybenzyl 2-hydroxy-4-methylpentanoate

HRID 1744112ノート

反応式

HRID 1744112 の反応式
[C:1]([OH:9])(=[O:8])[C@H:2]([CH2:4][CH:5]([CH3:7])[CH3:6])[OH:3].C([O-])([O-])=O.[Cs+].[Cs+].[CH3:16][O:17][C:18]1[CH:25]=[CH:24][C:21]([CH2:22]Cl)=[CH:20][CH:19]=1>CO.O.O>[OH:3][CH:2]([CH2:4][CH:5]([CH3:7])[CH3:6])[C:1]([O:9][CH2:22][C:21]1[CH:24]=[CH:25][C:18]([O:17][CH3:16])=[CH:19][CH:20]=1)=[O:8]

参加物

6

反応物 3

HCID 10796Cesium carbonateHCID 699934-Methyloxybenzyl chlorideHCID 83697Pentanoic acid, 2-hydroxy-4-methyl-, (2S)-

生成物 1

HCID 222360714-Methoxybenzyl 2-hydroxy-4-methylpentanoate

試薬・触媒・溶媒 2

HCID 962Water溶媒2 回HCID 22242641Methanol--water (1/1)溶媒

実験手順

To D/L-leucic acid (7.58 g, 57.36 mmol) in MeOH/H2O (9:1, 100 mL) was added a 20% solution of Cs2CO3 in water until the pH reached 7.0. The reaction mixture was concentrated in vacuo to dryness, DMF was added and concentrated in vacuo to dryness again. The solid was suspended in DMF (100 mL) at 0° C., 4-methoxybenzyl chloride (7.8 mL, 51.6 mmol) was added dropwise and the reaction mixture stirred overnight. The mixture was added to water and the product extracted with Et2O, dried over Na2SO4, concentrated in vacuo and purified by flash chromatography over silica gel (EtOAc/Hex, 2/8, then 3/7) to afford 4-methoxybenzyl 2-hydroxy-4-methylpentanoate.

後処理

  1. concentrationThe reaction mixture was concentrated in vacuo to dryness, DMF
  2. additionwas added
  3. concentrationconcentrated in vacuo to dryness again
  4. customwas suspended in DMF (100 mL) at 0° C.
  5. extractionthe product extracted with Et2O
  6. dry with materialdried over Na2SO4
  7. concentrationconcentrated in vacuo
  8. custompurified by flash chromatography over silica gel (EtOAc/Hex, 2/8

出典と根拠

ORDレコード
ord-59d54e1e08794ce98bb32f784255cbdb
出典データセット
uspto-grants-2006_03
特許番号
US07012075B2

反応ノート

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