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1,4-Diethyl 2-formylbutanedioate → HCID 178470733, 화합물

HRID 481420
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HRID 481420 반응식
[Na].Cl.[CH3:3][O:4][CH2:5][C:6]([NH2:8])=[NH:7].[CH:9]([CH:11]([CH2:17][C:18]([O:20][CH2:21][CH3:22])=[O:19])[C:12](OCC)=O)=[O:10]>C(O)C>[CH3:3][O:4][CH2:5][C:6]1[N:8]=[C:9]([OH:10])[C:11]([CH2:17][C:18]([O:20][CH2:21][CH3:22])=[O:19])=[CH:12][N:7]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 2315001,4-Diethyl 2-formylbutanedioateHCID 5360545SodiumHCID 135486022-Methoxyethanimidamide hydrochloride

생성물 1

HCID 178470733HCID 178470733, 화합물수율 43%

시약·촉매·용매 1

HCID 702Ethanol용매2회

실험 절차

Sodium metal (0.754 mol) was dissolved in absolute ethanol (100 ml) and the resulting solution was added dropwise to a solution of methoxyacetamidine hydrochloride (0.703 mol) in ethanol (100 ml). After 15 minutes the reaction mixture was filtered and the filtrate was added to a solution of diethyl formylsuccinate (0.703 mol), which was prepared according to H. Nakao et al. Ann. Sankyo Res. Lab., 18, 33-37 (1966). The reaction was refluxed for 15 hours, cooled to room temperature and was then concentrated to obtain a crude solid. This solid was crystallized from isopropanol to obtain the title compound (43% yield), m.p. 142°-143° C.

후처리

  1. filtrationAfter 15 minutes the reaction mixture was filtered
  2. customwas prepared
  3. temperatureThe reaction was refluxed for 15 hours
  4. concentrationwas then concentrated
  5. customto obtain a crude solid
  6. customThis solid was crystallized from isopropanol

출처 및 근거

ORD 기록
ord-587b3e7e02fd4e9f9937e0fcba93834b
출처 데이터셋
uspto-grants-1998_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05789415

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