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Water → HCID 21243569, 화합물

HRID 621814
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HRID 621814 반응식
[CH3:1][C:2](C)([O-])[CH3:3].[K+].[OH:7][C:8]1[CH:12]=[C:11]([CH3:13])[O:10][C:9]=1[C:14]([O:16][CH2:17][CH3:18])=[O:15].BrC(C)C.O>CS(C)=O>[CH3:13][C:11]1[O:10][C:9]([C:14]([O:16][CH2:17][CH3:18])=[O:15])=[C:8]([O:7][CH:2]([CH3:3])[CH3:1])[CH:12]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 962WaterHCID 63582-BromopropaneHCID 23665647Potassium tert-butoxideHCID 54697152HCID 54697152, 화합물

생성물 1

HCID 21243569HCID 21243569, 화합물수율 68%

시약·촉매·용매 1

HCID 679Dimethyl Sulfoxide용매2회

실험 절차

A solution of 1.6 g (14.3 mmol, 1.2 equiv) of potassium tert-butoxide in 11 mL of dimethyl sulfoxide is added to a solution of 2.0 g (11.8 mmol) of ethyl 3-hydroxy-5-methyl-2-furancarboxylate (Takei, H. and Mukaiyama, T., Bull. Soc. Chem. Jpn., 43, 3607 (1970)) in 40 mL of dimethyl sulfoxide under a nitrogen atmosphere. The resulting solution is stirred at room temperature for 1 hour and treated with 5.9 g (47.9 mmol, 4.1 equiv) of 2-bromopropane. The reaction is stirred at room temperature for 7.5 hours under nitrogen and poured onto 100 mL of water. The aqueous solution is extracted with ethyl acetate (4x). The combined extracts are washed with water (2x) and saturated aqueous sodium chloride, dried over sodium sulfate and concentrated in vacuo to give 1.7 g (2.5 g theo., 68%) of ethyl 5-methyl-3-isopropoxy-2-furancarboxylate as a pale, yellow oil.

후처리

  1. stirringThe reaction is stirred at room temperature for 7.5 hours under nitrogen
  2. extractionThe aqueous solution is extracted with ethyl acetate (4x)
  3. washThe combined extracts are washed with water (2x) and saturated aqueous sodium chloride
  4. dry with materialdried over sodium sulfate
  5. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-98d675ebfef149ba91c0a85005df149d
출처 데이터셋
uspto-grants-1989_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04824958

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