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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Sulfuric Acid → 4-Hydroxy-3-methyl-2-pentyl-cyclopent-2-enone

HRID 365169
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반응식

HRID 365169 반응식
C(O[C:5]1([CH3:16])[CH:9]=[CH:8][C:7](=[O:10])[CH:6]1[CH2:11][CH2:12][CH2:13][CH2:14][CH3:15])(=O)C.S(=O)(=O)(O)[OH:18]>O1CCCC1>[OH:18][CH:9]1[CH2:8][C:7](=[O:10])[C:6]([CH2:11][CH2:12][CH2:13][CH2:14][CH3:15])=[C:5]1[CH3:16]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 1118Sulfuric AcidHCID 135172551-Methyl-4-oxo-5-pentylcyclopent-2-EN-1-YL acetate

생성물 1

HCID 122257564-Hydroxy-3-methyl-2-pentyl-cyclopent-2-enone

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

In the same flask as in Example 1, there were charged 3-acetoxy-2-n-pentyl-3-methyl-4-cyclopentenone (2.24 g), tetrahydrofuran (10 ml) and 20% sulfuric acid (10 ml), and the resultant mixture was stirred at 30° to 50° C. for 6 hours. After completion of the reaction, the reaction mixture was subjected to post-treatment and purification as in example 1 to give 1.55 g of 4-hydroxy-2-n-pentyl-3-methyl-2-cyclopentenone. Yield, 85%.

후처리

  1. customAfter completion of the reaction
  2. custompurification as in example 1

출처 및 근거

ORD 기록
ord-e3c22cd44e024245bfdac5e1d30226cb
출처 데이터셋
uspto-grants-1986_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04608442

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