홈MCP워크벤치Skills
홈워크벤치알림마이페이지
llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
  1. 홈
  2. /반응

Sodium Hydroxide → HCID 58431987, 화합물

HRID 1798594
노트
인쇄 미리보기

반응식

HRID 1798594 반응식
[O:1]=[S:2]1(=[O:20])[CH2:6][CH2:5][CH2:4][N:3]1[C:7]1[CH:12]=[CH:11][C:10]([CH:13]([O:18][CH3:19])[C:14]([O:16]C)=[O:15])=[CH:9][CH:8]=1.[OH-].[Na+]>CO>[O:1]=[S:2]1(=[O:20])[CH2:6][CH2:5][CH2:4][N:3]1[C:7]1[CH:8]=[CH:9][C:10]([CH:13]([O:18][CH3:19])[C:14]([OH:16])=[O:15])=[CH:11][CH:12]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 14798Sodium HydroxideHCID 58432115HCID 58432115, 화합물

생성물 1

HCID 58431987HCID 58431987, 화합물수율 82.8%

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

To a solution of methyl 2-(4-(1,1-dioxidoisothiazolidin-2-yl)phenyl)-2-methoxyacetate (0.48 g, 1.6 mmol) in MeOH (21 mL) was added 1 M NaOH (7 mL, 7 mmol) slowly. After stirring at room temperature for 23 hrs, the volatiles were removed in vacuo and the residue was dissolved in H2O. EtOAc was added to the aqueous solution and saturated aqueous NH4Cl and 1 M HCl were added slowly until the pH ˜3. The mixture was extracted with EtOAc then the aqueous layer was acidified to pH 1 and extracted with EtOAc again. The combined organics were washed with H2O and brine, dried over Na2SO4 and concentrated in vacuo to give 2-(4-(1,1-dioxidoisothiazolidin-2-yl)phenyl)-2-methoxyacetic acid as a yellow foam (0.378 g, 82% yield). The product was used in the next synthetic step without further purification.

후처리

  1. customthe volatiles were removed in vacuo
  2. dissolutionthe residue was dissolved in H2O
  3. additionEtOAc was added to the aqueous solution and saturated aqueous NH4Cl and 1 M HCl
  4. additionwere added slowly until the pH ˜3
  5. extractionThe mixture was extracted with EtOAc
  6. extractionextracted with EtOAc again
  7. washThe combined organics were washed with H2O and brine
  8. dry with materialdried over Na2SO4
  9. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-de8c15a3817247abbc02386f6fcd026b
출처 데이터셋
uspto-grants-2013_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08343970B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트