Sodium Perborate → 3-Methoxy-2-(methoxymethyl)propan-1-ol

HRID 252048

反応式

HRID 252048 の反応式
[CH3:1][O:2][CH2:3][C:4]([CH2:6][O:7][CH3:8])=[CH2:5].B.C1C[O:13]CC1.B(O[O-])=O.[Na+]>C1COCC1.C(Cl)Cl>[CH3:1][O:2][CH2:3][CH:4]([CH2:6][O:7][CH3:8])[CH2:5][OH:13]

参加物

6

実験手順

To a solution of the 3-methoxy-2-methoxymethyl-1-propene (3.5 g, 30 mmol, 1.0 eq.) in THF (10 mL) at 0° C. was added BH3.THF (1M in THF, 18 mL, 0.6 eq.) and the resulting mixture was stirred for 40 min. The reaction was quenched with water followed by sodium perborate (10.6 g, 2.3 eq.), warmed to room temperature, stirred overnight, diluted with CH2Cl2 and filtered through celite. The filtrate was diluted with brine and the separated aqueous layer was extracted with CH2Cl2. The combined extracts were dried over Na2SO4 and filtered. The filtrate was distilled at atmospheric pressure to give light yellow liquid residue. Fractional distillation of the residue at 40 milliTorr gave 3-methoxy-2-methoxymethypropan-1-ol (1.93 g, 48%). b.p.=90-110° C.

後処理

  1. customThe reaction was quenched with water
  2. stirringstirred overnight
  3. filtrationfiltered through celite
  4. additionThe filtrate was diluted with brine
  5. extractionthe separated aqueous layer was extracted with CH2Cl2
  6. dry with materialThe combined extracts were dried over Na2SO4
  7. filtrationfiltered
  8. distillationThe filtrate was distilled at atmospheric pressure
  9. customto give light yellow liquid residue
  10. distillationFractional distillation of the residue at 40 milliTorr

出典と根拠

ORDレコード
ord-49d4b571b92f41cb97b126f1cf931465
出典データセット
uspto-grants-2011_01
特許番号
US07868002B2

関連ノート

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