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N-Hydroxysuccinimide → 2,5-Dioxopyrrolidin-1-yl 2-methoxyacetate

HRID 1753109
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HRID 1753109 반응식
[CH3:1][O:2][CH2:3][C:4](Cl)=[O:5].[OH:7][N:8]1[C:12](=[O:13])[CH2:11][CH2:10][C:9]1=[O:14].C([O-])(O)=O.[Na+]>ClCCl>[CH3:1][O:2][CH2:3][C:4]([O:7][N:8]1[C:12](=[O:13])[CH2:11][CH2:10][C:9]1=[O:14])=[O:5]
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참가 물질

5

반응물 3

HCID 80170N-HydroxysuccinimideHCID 96623Methoxyacetyl chlorideHCID 516892Sodium Bicarbonate

생성물 1

HCID 103524272,5-Dioxopyrrolidin-1-yl 2-methoxyacetate수율 79%

시약·촉매·용매 1

HCID 6344Dichloromethane용매2회

실험 절차

A solution of methoxyacetyl chloride (108.5 g, 1 mol) in absolute dichloromethane (170 mL) was added dropwise at 0° C. to a solution of N-hydroxysuccinimide (115 g, 1 mol) and TEA (111 g, 1 mol) in dichloromethane (900 mL). The reaction mixture was stirred at room temperature for 48 hours, and a saturated NaHCO3 solution (500 mL) was added under stirring. The organic layer was separated, and the aqueous layer was subjected to extraction twice with chloroform. The combined organic extract was washed with saturated NaHCO3 solution (200 mL), brine (200 mL), and dried over Na2SO4. The solution was concentrated in vacuo to afford the title compound as a yellow oil (147.8 g, 79%). Taken directly on to the next step.

후처리

  1. stirringunder stirring
  2. customThe organic layer was separated
  3. extractionthe aqueous layer was subjected to extraction twice with chloroform
  4. extractionThe combined organic extract
  5. washwas washed with saturated NaHCO3 solution (200 mL), brine (200 mL)
  6. dry with materialdried over Na2SO4
  7. concentrationThe solution was concentrated in vacuo

출처 및 근거

ORD 기록
ord-6845c8b53cd246d0a9c7c12ce0acc910
출처 데이터셋
uspto-grants-2015_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09163021B2

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