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Propylene Oxide → alpha-Methyl-2-furanethanol

HRID 900437
ノート
印刷プレビュー

反応式

HRID 900437 の反応式
[O:1]1[CH:5]=[CH:4][CH:3]=[CH:2]1.C([Li])CCC.[CH2:11]1[O:14][CH:12]1[CH3:13]>O1CCCC1>[O:1]1[CH:5]=[CH:4][CH:3]=[C:2]1[CH2:11][CH:12]([OH:14])[CH3:13]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 6378Propylene OxideHCID 8029FuranHCID 178418339Butyllithium

生成物 1

HCID 10855456alpha-Methyl-2-furanethanol

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

実験手順

To a solution of furan (7.93 g) in tetrahydrofuran (100 ml) cooled to 5° C. was added dropwise n-butyl lithium (80.2 ml, 1.6M in hexanes). The mixture was stirred for 2 h. A solution of propylene oxide (12.2 ml) was added dropwise and the resulting mixture was stirred at 0° C. for 1 h. The reaction mixture was quenched with saturated ammonium chloride and extracted with diethyl ether. The organics were dried (MgSO4) and concentrated. The crude oil was distilled to give 1-(2-furyl)-propan-2-ol (3.85 g, b.p. 68-70° C. at 6.0 mm).

後処理

  1. stirringthe resulting mixture was stirred at 0° C. for 1 h
  2. customThe reaction mixture was quenched with saturated ammonium chloride
  3. extractionextracted with diethyl ether
  4. dry with materialThe organics were dried (MgSO4)
  5. concentrationconcentrated
  6. distillationThe crude oil was distilled

出典と根拠

ORDレコード
ord-d72e89fe53f54547a35b54881864a80b
出典データセット
uspto-grants-2008_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07358376B2

反応ノート

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