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4,5-Dihydro-2-(methylthio)thiazole → 1-(4,5-Dihydrothiazol-2-yl)azetidin-3-ol

HRID 1419464
ノート
印刷プレビュー

反応式

HRID 1419464 の反応式
Cl.[OH:2][CH:3]1[CH2:6][NH:5][CH2:4]1.CS[C:9]1[S:10][CH2:11][CH2:12][N:13]=1.C[O-].[Na+]>C(O)C>[OH:2][CH:3]1[CH2:6][N:5]([C:9]2[S:10][CH2:11][CH2:12][N:13]=2)[CH2:4]1
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 883244,5-Dihydro-2-(methylthio)thiazole2 回HCID 27592903-Hydroxyazetidine hydrochloride2 回HCID 10942334Sodium Methoxide

生成物 1

HCID 109865151-(4,5-Dihydrothiazol-2-yl)azetidin-3-ol収率 81.5%

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒

実験手順

To a solution of 109 mg of 3-hydroxyazetidine HCl [Compound (15)] in 5 ml of ethanol was added a mixture of 133 mg of 2-methylthiothiazoline [Compound (16)] and sodium methoxide (0.9 equivalent mole), and the reaction mixture was refluxed for 8 hours. After removal of the solvent under reduced pressure, the resulting residue was dissolved in chloroform and washed with saturated saline solution. After removal of the solvent under reduced pressure, the resulting residue was washed with diethylether to give 119 mg (81.5%) of 3-hydroxy-1-(thiazolin-2-yl)azetidine [Compound (17)] as crystals.

後処理

  1. temperaturethe reaction mixture was refluxed for 8 hours
  2. customAfter removal of the solvent under reduced pressure
  3. dissolutionthe resulting residue was dissolved in chloroform
  4. washwashed with saturated saline solution
  5. customAfter removal of the solvent under reduced pressure
  6. washthe resulting residue was washed with diethylether

出典と根拠

ORDレコード
ord-4ac4a670b0e74c919204719ffebfd63a
出典データセット
uspto-grants-1999_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05886172

反応ノート

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