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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Ethyl propiolate → Ethyl 1-benzyl-1H-pyrrole-3-carboxylate

HRID 51231
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반응식

HRID 51231 반응식
[CH2:1]([N:8]([CH:13]=O)[CH2:9][C:10](O)=O)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[C:15]([O:19][CH2:20][CH3:21])(=[O:18])[C:16]#C>C(OC(=O)C)(=O)C>[CH2:1]([N:8]1[CH:9]=[CH:10][C:16]([C:15]([O:19][CH2:20][CH3:21])=[O:18])=[CH:13]1)[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 12182Ethyl propiolateHCID 12958481N-benzyl-N-formylglycine

생성물 1

HCID 14667729Ethyl 1-benzyl-1H-pyrrole-3-carboxylate수율 94%

시약·촉매·용매 1

HCID 7918Acetic Anhydride용매

실험 절차

Using 1.93 g (10 mmol) of N-benzyl-N-formylglycine, 3.65 g (37.2 mmol) of ethyl propiolate and 10 ml of acetic anhydride, a reaction and post treatment were conducted in a similar manner as in Referential Example 1. The resulting brown oil was purified by silica gel column chromatography [silica gel: “No.9385”, product of Merck & Co., Inc. (the same silica gel was also used in the subsequent referential examples and examples); eluent: ethyl acetate/hexane=1/3], whereby 2.156 g of the title compound were obtained (yield: 94.0%).

후처리

  1. customa reaction and post treatment
  2. customThe resulting brown oil was purified by silica gel column chromatography [silica gel

출처 및 근거

ORD 기록
ord-e0fa7bb7423b45bc8f58fa72baab2e22
출처 데이터셋
uspto-grants-2004_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06713634B2

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