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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Diethyl Ether → HCID 21866824, 화합물

HRID 1796348
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HRID 1796348 반응식
CCOCC.[H-].[Al+3].[Li+].[H-].[H-].[H-].[Cl:12][CH2:13][CH2:14][CH2:15][CH2:16][CH:17]([C:23](OCC)=[O:24])[C:18](OCC)=[O:19].[OH-].[Na+]>O.O1CCCC1>[Cl:12][CH2:13][CH2:14][CH2:15][CH2:16][CH:17]([CH2:23][OH:24])[CH2:18][OH:19]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 4

HCID 3283Diethyl Ether2회HCID 14798Sodium HydroxideHCID 21226445Aluminium lithium hydrideHCID 53401795Diethyl 2-(4-chlorobutyl)malonate

생성물 1

HCID 21866824HCID 21866824, 화합물수율 102.6%

시약·촉매·용매 2

HCID 962Water용매2회

실험 절차

To 214 ml of dry ether was added 8 g of lithium aluminium hydride, and a solution of 26.7 g of diethyl (4-chlorobutyl)malonate/53 ml of dry ether was added dropwise with stirring under ice-cooling. After 1-hour-stirring at room temperature, the mixture was cooled with ice-cold water, and 173 ml of tetrahydrofuran/14.7 ml of water was added gradually. Then, 14.7 ml of 1N sodium hydroxide solution and 35 ml of water were added, stirred for 15 minutes, filtrated to remove insolubles. The filtrate was concentrated to provide 18.2 g of the objective compound as colorless oil.

후처리

  1. temperaturecooling
  2. stirringAfter 1-hour-stirring at room temperature
  3. additionwas added gradually
  4. stirringstirred for 15 minutes
  5. filtrationfiltrated
  6. customto remove insolubles
  7. concentrationThe filtrate was concentrated

출처 및 근거

ORD 기록
ord-2c0409bfb3e34df399a9b8acceee9f57
출처 데이터셋
uspto-grants-2006_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07030143B2

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이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트
HCID 8028
Tetrahydrofuran
용매