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Water → Ethyl 5-methylfuran-3-carboxylate

HRID 1952855
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HRID 1952855 반응식
[CH:1]([CH:3]([CH2:9][C:10]([CH3:12])=[O:11])[C:4]([O:6][CH2:7][CH3:8])=[O:5])=O.O>C1C=CC=CC=1>[CH3:12][C:10]1[O:11][CH:1]=[C:3]([C:4]([O:6][CH2:7][CH3:8])=[O:5])[CH:9]=1
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참가 물질

4

반응물 2

HCID 962WaterHCID 23301347Ethyl 2-formyl-4-oxopentanoate

생성물 1

HCID 12332585Ethyl 5-methylfuran-3-carboxylate

시약·촉매·용매 1

HCID 241Benzene용매

실험 절차

The abovementioned mixture of ethyl 2-formyllevulinate and its diethyl ketal was dissolved in benzene, the catalyst was added, and the resulting solution was refluxed with a Dean-Stark trap for 3-3.5 h until the water was completely removed. The reaction mixture was then distilled under reduced pressure, resulting in 15 g (97 mmol) of ethyl 5-methylfuran-3-carboxylate, boiling point 97° C./15 mm Hg.

후처리

  1. additionthe catalyst was added
  2. customwas completely removed
  3. distillationThe reaction mixture was then distilled under reduced pressure

출처 및 근거

ORD 기록
ord-7cf28bb1cf2a4723afdebdb54eda7538
출처 데이터셋
uspto-grants-2000_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06114358

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