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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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N-methyl-2-pyrrolidone → HCID 72988237, 화합물

HRID 1992755
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인쇄 미리보기

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HRID 1992755 반응식
[CH3:1][O:2][CH:3]([O:20][CH3:21])[CH2:4][CH:5]1[C:9](=[O:10])[CH2:8][CH2:7][CH:6]1[CH:11](C(OC)=O)[C:12]([O:14][CH3:15])=[O:13].CN1C(=O)CCC1>O>[CH3:1][O:2][CH:3]([O:20][CH3:21])[CH2:4][CH:5]1[C:9](=[O:10])[CH2:8][CH2:7][CH:6]1[CH2:11][C:12]([O:14][CH3:15])=[O:13]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 13387N-methyl-2-pyrrolidoneHCID 67423893HCID 67423893, 화합물

생성물 1

HCID 72988237HCID 72988237, 화합물수율 81%

시약·촉매·용매 1

HCID 962Water용매

실험 절차

In a 3-neck 250 ml round bottom flask equipped with a short path distillation apparatus, a solution of 80.0 g of dimethyl [2-(2,2-dimethoxyethyl)-3-oxocyclopentyl]malonate and 63.0 g NMP was heated to 160° C. The solution was then charged with water until the reaction was complete. Upon completion of the reaction, distillation under vacuum (b.p.=140-145° C. at 1 mbar) of the reaction medium allowed to recover directly the purified title compound with a yield of 81%.

후처리

  1. customIn a 3-neck 250 ml round bottom flask equipped with a short path distillation apparatus
  2. customUpon completion of the reaction, distillation under vacuum (b.p.=140-145° C. at 1 mbar) of the reaction medium
  3. customto recover directly the
  4. custompurified title compound with a yield of 81%

출처 및 근거

ORD 기록
ord-19597ef50be54893ac27967911088bd7
출처 데이터셋
uspto-grants-2010_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07649107B2

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