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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Diethyl octylmalonate → 2-Octylpropane-1,3-diol

HRID 1197381
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HRID 1197381 반응식
[H-].[Al+3].[Li+].[H-].[H-].[H-].[CH2:7]([CH:15]([C:21](OCC)=[O:22])[C:16](OCC)=[O:17])[CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH3:14].O.C1COCC1>CCOCC>[CH2:7]([CH:15]([CH2:16][OH:17])[CH2:21][OH:22])[CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH3:14]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 252340Diethyl octylmalonateHCID 21226445Aluminium lithium hydride2회HCID 21881883Oxolane--water (1/1)

생성물 1

HCID 3160622-Octylpropane-1,3-diol수율 65%

시약·촉매·용매 1

HCID 3283Diethyl Ether용매3회

실험 절차

250 ml of ether and 19.0 of lithium aluminum hydride were put in a 1-liter four-necked flask, and a solution obtained by dissolving 72.1 g of the thus prepared diethyl octylmalonate in 50 ml of ether was put therein dropwise at such a rate that ether is gently refluxed. After the dropwise addition, the mixture was refluxed with heating for 3 hours, and after allowing it to cool, a mixture of water-THF was added to decompose excess lithium aluminum hydride. The resultant solid was removed by filtration, and the filtrate was washed with saturated saline and dried over anhydrous sodium sulfate. The crude crystal obtained by distilling away the solvents was recrystallized from isooctane to give 32.4 g of colorless crystals. Yield 65%.

후처리

  1. customa solution obtained
  2. additionAfter the dropwise addition
  3. temperaturethe mixture was refluxed
  4. temperaturewith heating for 3 hours
  5. temperatureto cool
  6. additionwas added
  7. customThe resultant solid was removed by filtration
  8. washthe filtrate was washed with saturated saline
  9. dry with materialdried over anhydrous sodium sulfate
  10. customThe crude crystal obtained
  11. distillationby distilling away the solvents
  12. customwas recrystallized from isooctane

출처 및 근거

ORD 기록
ord-75f5a8e07c7d480386493afe3e8dc376
출처 데이터셋
uspto-grants-1994_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05275757

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