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

HRID 2411140
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HRID 2411140 반응식
[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
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참가 물질

6

반응물 2

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

생성물 1

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

시약·촉매·용매 3

HCID 887Methanol용매HCID 8028Tetrahydrofuran용매
HCID 14798
Sodium Hydroxide
용매

실험 절차

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).

후처리

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

출처 및 근거

ORD 기록
ord-11b1acc7583545b7bc4bea2df16a3331
출처 데이터셋
uspto-grants-2014_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08816079B2

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