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2-Iodophenol → 4-(2-Iodophenoxymethyl)-1-methyl-1,2,3,6-tetrahydropyridine

HRID 1872070
ノート
印刷プレビュー

反応式

HRID 1872070 の反応式
[OH:1][CH2:2][C:3]1[CH2:4][CH2:5][N:6]([CH3:9])[CH2:7][CH:8]=1.[I:10][C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][C:12]=1O.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.N(C(OCC)=O)=NC(OCC)=O>C1COCC1>[I:10][C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][C:12]=1[O:1][CH2:2][C:3]1[CH2:8][CH2:7][N:6]([CH3:9])[CH2:5][CH:4]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 107842-IodophenolHCID 11776TriphenylphosphineHCID 1189211,2,3,6-Tetrahydro-1-methylpyridine-4-methanolHCID 220568ethyl N-ethoxycarbonyliminocarbamate

生成物 1

HCID 107350934-(2-Iodophenoxymethyl)-1-methyl-1,2,3,6-tetrahydropyridine収率 66.4%

試薬・触媒・溶媒 1

HCID 8028
Tetrahydrofuran
溶媒

実験手順

4-(Hydroxymethyl)-1-methyl-1,2,3,6-tetrahydropyridine (D1, 5.63 g, 0.044 mol), 2-iodophenol (7.80 g, 0.035 mol) and triphenylphosphine (11.61 g, 0.044 mol) were stirred in dry THF (200 ml) under Ar as diethyl azodicarboxylate (7.0 ml, 0.044 mol) was added portionwise. The solution was stirred for 1h, concentrated, diluted with ethyl acetate, and extracted with dil. HCl. The extract was basified (sat. K2CO3 solution) and extracted with ethyl acetate. This organic extract was dried (Na2SO4) and evaporated to give a brown oil. Purification by chromatography on silica gel, eluting with 0-10% methanol/chloroform (gradient) gave the title compound (7.65 g, 65%) as an amber oil.

後処理

  1. additionwas added portionwise
  2. concentrationconcentrated
  3. additiondiluted with ethyl acetate
  4. extractionextracted with dil. HCl
  5. extractionextracted with ethyl acetate
  6. extractionThis organic extract
  7. dry with materialwas dried (Na2SO4)
  8. customevaporated
  9. customto give a brown oil
  10. customPurification by chromatography on silica gel
  11. washeluting with 0-10% methanol/chloroform (gradient)

出典と根拠

ORDレコード
ord-f5f3acea63a24f60ba3badd02efc1672
出典データセット
uspto-grants-2000_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06107328

反応ノート

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