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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Water → 4-(4-Methylphenyl)butanol

HRID 1479268
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인쇄 미리보기

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HRID 1479268 반응식
[H-].[Al+3].[Li+].[H-].[H-].[H-].[CH3:7][C:8]1[CH:13]=[CH:12][C:11]([CH2:14][CH2:15][CH2:16][C:17](O)=[O:18])=[CH:10][CH:9]=1.O.[OH-].[Na+]>CCOCC>[CH3:7][C:8]1[CH:13]=[CH:12][C:11]([CH2:14][CH2:15][CH2:16][CH2:17][OH:18])=[CH:10][CH:9]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 962Water2회HCID 14798Sodium HydroxideHCID 782794-p-Tolylbutyric acidHCID 21226445Aluminium lithium hydride

생성물 1

HCID 1040094-(4-Methylphenyl)butanol

시약·촉매·용매 1

HCID 3283Diethyl Ether용매2회

실험 절차

To lithium aluminum hydride (427 mg, 11.2 mmol) suspended in dry ether (5 ml) at 0° C. is added 1 g of 4-(4-methylphenyl)butanoic acid (5.614 mmol) dissolved in dry ether (10 ml) over a period of 30 minutes. The reaction mixture is then allowed to warm to room temperature and stirred for 4 hours. Water (0.43 ml), NaOH (15% solution, 0.43 g) and water (1.29 ml) were then added successively and the resulting solution is stirred for 30 minutes. The resulting precipitate is filtered and washed with ether and dried. The filtrate is then concentrated and purified by flash chromatography using ethyl acetate-hexanes as the eluting medium.

후처리

  1. stirringthe resulting solution is stirred for 30 minutes
  2. filtrationThe resulting precipitate is filtered
  3. washwashed with ether
  4. customdried
  5. concentrationThe filtrate is then concentrated
  6. custompurified by flash chromatography

출처 및 근거

ORD 기록
ord-cc6f07d03f6f4eb9b51fa0bfbbe89f0c
출처 데이터셋
uspto-grants-2016_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09408927B2

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