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Hydrochloric Acid → 5-(2-Methylphenyl)-5-oxovaleric acid

HRID 322985
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반응식

HRID 322985 반응식
[C:1]1(=[O:8])[O:7][C:5](=[O:6])[CH2:4][CH2:3][CH2:2]1.[CH3:9][C:10]1[CH:15]=[CH:14][CH:13]=[CH:12][C:11]=1[Mg]Cl.Cl>O1CCCC1>[O:6]=[C:5]([C:11]1[CH:12]=[CH:13][CH:14]=[CH:15][C:10]=1[CH3:9])[CH2:4][CH2:3][CH2:2][C:1]([OH:7])=[O:8]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 313Hydrochloric AcidHCID 7940Glutaric anhydrideHCID 178424304HCID 178424304, 화합물

생성물 1

HCID 27600035-(2-Methylphenyl)-5-oxovaleric acid

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매2회

반응 조건

온도
-78 °C

실험 절차

A stirred solution of glutaric anhydride (22.82 g) in dry tetrahydrofuran (300 mL) at −78° C. is treated with a solution of 2-methylphenyl magnesium chloride in tetrahydrofuran (200 mL, 0.1 M) over 45 minutes. The mixture is stirred at −78° C. for 2.5 hours and the grey suspension is poured into 1 N hydrochloric acid (300 mL). The mixture is extracted with ethyl acetate (300 mL). The organic phase is dried over magnesium sulphate and evaporated to give 5-oxo-5-(2-methylphenyl)pentanoic acid (36.74 g) as a red-brown oil.

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

후처리

  1. extractionThe mixture is extracted with ethyl acetate (300 mL)
  2. dry with materialThe organic phase is dried over magnesium sulphate
  3. customevaporated

출처 및 근거

ORD 기록
ord-9a5a2d605f79416ea8c4086a1bbb5d8b
출처 데이터셋
uspto-grants-2001_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06211234B1

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