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Hydrochloric Acid → 4-(1,1-Dioxo-1lambda6-isothiazolidin-2-ylmethyl)benzoic acid

HRID 2411140
ノート
印刷プレビュー

反応式

HRID 2411140 の反応式
[O:1]=[S:2]1(=[O:18])[CH2:6][CH2:5][CH2:4][N:3]1[CH2:7][C:8]1[CH:17]=[CH:16][C:11]([C:12]([O:14]C)=[O:13])=[CH:10][CH:9]=1.Cl>O1CCCC1.CO.[OH-].[Na+]>[O:1]=[S:2]1(=[O:18])[CH2:6][CH2:5][CH2:4][N:3]1[CH2:7][C:8]1[CH:17]=[CH:16][C:11]([C:12]([OH:14])=[O:13])=[CH:10][CH:9]=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 2

HCID 313Hydrochloric AcidHCID 43620001Methyl 4-(1,1-dioxo-1lambda6-isothiazolidin-2-ylmethyl)benzoate

生成物 1

HCID 246888894-(1,1-Dioxo-1lambda6-isothiazolidin-2-ylmethyl)benzoic acid収率 87.6%

試薬・触媒・溶媒 3

HCID 887Methanol溶媒HCID 8028Tetrahydrofuran溶媒
HCID 14798
Sodium Hydroxide
溶媒

実験手順

Methyl 4-(1,1-dioxo-1λ6-isothiazolidin-2-ylmethyl)benzoate (1.95 g) described in Preparation Example 17 was dissolved in a solution of tetrahydrofuran (20 mL) and methanol (20 mL), 1N aqueous sodium hydroxide solution was added, and the mixture was stirred at room temperature. The reaction mixture was neutralized with 1N hydrochloric acid, and the solvent was evaporated. To the obtained residue was added water, and the insoluble material was collected by filtration to give the title compound (1.62 g).

後処理

  1. additionwas added
  2. customthe solvent was evaporated
  3. additionTo the obtained residue was added water
  4. filtrationthe insoluble material was collected by filtration

出典と根拠

ORDレコード
ord-11b1acc7583545b7bc4bea2df16a3331
出典データセット
uspto-grants-2014_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08816079B2

反応ノート

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