2-Chloroethanol → 2-(5-Iodo-indol-1-yl)-ethanol

HRID 1916706

反応式

HRID 1916706 の反応式
[I:1][C:2]1[CH:3]=[C:4]2[C:8](=[CH:9][CH:10]=1)[NH:7][CH:6]=[CH:5]2.[OH-].[K+].Cl[CH2:14][CH2:15][OH:16].CCOC(C)=O>CS(C)=O>[I:1][C:2]1[CH:3]=[C:4]2[C:8](=[CH:9][CH:10]=1)[N:7]([CH2:14][CH2:15][OH:16])[CH:6]=[CH:5]2

参加物

6

反応物 4

HCID 342-ChloroethanolHCID 8857Ethyl AcetateHCID 14797Potassium HydroxideHCID 27823135-Iodo-1H-indole

生成物 1

HCID 457893802-(5-Iodo-indol-1-yl)-ethanol

試薬・触媒・溶媒 1

HCID 679Dimethyl Sulfoxide溶媒2 回

実験手順

Under an N2 atmosphere 30 g (121 mmol) 5-iodoindole are added to a suspension of 27.1 g (484 mmol) KOH in 150 mL DMSO. The reaction mixture is kept for 1 h at RT, cooled to 0° C. with ice water, 9.7 mL (145 mmol) of 2-chloroethanol in 30 mL DMSO are slowly added dropwise and stirred for 4.5 h at RT. The reaction mixture is combined with 1 L EtOAc, washed four times with in each case 800 mL water and once with 400 mL saturated NaCl solution and the organic phase is dried over Na2SO4. After the desiccant and solvent have been eliminated the residue is purified by chromatography (silica gel, cyc/EtOAc 3:1).

後処理

  1. additionare slowly added dropwise
  2. washwashed four times with in each case 800 mL water
  3. dry with materialonce with 400 mL saturated NaCl solution and the organic phase is dried over Na2SO4
  4. customis purified by chromatography (silica gel, cyc/EtOAc 3:1)

出典と根拠

ORDレコード
ord-6dde589b709a42c683272ae1e51fa024
出典データセット
uspto-grants-2013_12
特許番号
US08618132B2

関連ノート

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