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Allyl iodide → Butyl 1-allylcyclopropane-1-sulfonate

HRID 73393
ノート
印刷プレビュー

反応式

HRID 73393 の反応式
[CH:1]1([S:4]([O:7][CH2:8][CH2:9][CH2:10][CH3:11])(=[O:6])=[O:5])[CH2:3][CH2:2]1.[CH2:12]([Li])[CH2:13][CH2:14]C.C(I)C=C>C1COCC1>[CH2:14]([C:1]1([S:4]([O:7][CH2:8][CH2:9][CH2:10][CH3:11])(=[O:6])=[O:5])[CH2:3][CH2:2]1)[CH:13]=[CH2:12]
参加物反応条件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 11166Allyl iodideHCID 10464888Butyl cyclopropanesulfonateHCID 178418339Butyllithium

生成物 1

HCID 59386376Butyl 1-allylcyclopropane-1-sulfonate収率 69%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

反応条件

温度
-78 °C

実験手順

To a solution of 1-butyl cyclopropanesulfonate (4.8 g, 24.9 mmol) in THF at −78° C. was added simultaneously butyllithium solution (15.6 ml, 24.9 mmol, 1.6M, THF) and allyl iodide (24.9 mmol) under nitrogen atmosphere. The reaction mixture was stirred 2 hours at −78° C. and 3 hours at room temperature. The volatiles were evaporated under reduced pressure and the residue extracted with CH2Cl2 (100 ml). The extract was washed with water, dried (MgSO4) and evaporated. The residue was purified over silica gel chromatography (eluants: hexane/CH2Cl2) to obtain the titled product (3.75 g, 69.0%) as a colorless oil, 1H NMR (300 MHz, CDCl3): δ 5.6 (m, 1H), 5.13-5.08 (t, 2H), 4.21 (t, 2H), 2.65 (d, 2H), 1.7 (m, 2H), 1.4 (m, 4H), 0.93 (m, 5H).

後処理

  1. customThe volatiles were evaporated under reduced pressure
  2. extractionthe residue extracted with CH2Cl2 (100 ml)
  3. washThe extract was washed with water
  4. dry with materialdried (MgSO4)
  5. customevaporated
  6. customThe residue was purified over silica gel chromatography (eluants: hexane/CH2Cl2)

出典と根拠

ORDレコード
ord-d91d8ed404e84d39b56aac3d09d5d6d1
出典データセット
uspto-grants-2014_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08829052B2

反応ノート

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