홈MCP워크벤치Skills
홈워크벤치알림마이페이지
llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
  1. 홈
  2. /반응

Water → 1,3-Propanediol, 2-(2,2-dimethoxyethyl)-

HRID 2291844
노트
인쇄 미리보기

반응식

HRID 2291844 반응식
[CH3:1][O:2][CH:3]([O:16][CH3:17])[CH2:4][CH:5]([C:11](OCC)=[O:12])[C:6](OCC)=[O:7].[H-].[Al+3].[Li+].[H-].[H-].[H-].O.[OH-].[Na+]>CCOCC>[CH3:17][O:16][CH:3]([O:2][CH3:1])[CH2:4][CH:5]([CH2:11][OH:12])[CH2:6][OH:7]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 962Water2회HCID 14798Sodium HydroxideHCID 14215238Diethyl (2,2-dimethoxyethyl)malonateHCID 21226445Aluminium lithium hydride

생성물 1

HCID 117895481,3-Propanediol, 2-(2,2-dimethoxyethyl)-수율 66.5%

시약·촉매·용매 1

HCID 3283Diethyl Ether
이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트
용매

실험 절차

Diethyl (2,2-dimethoxyethyl)malonate (115.0 g, 0.46 mol) was added to a suspension of lithium aluminum hydride (38.0 g, 1.00 mol) in 400 ml of dry ether at a rate to maintain a gentle reflux. After stirring for 15 min. 40 ml of water, 40 ml of 15% aqueous NaOH, and 120 ml of water were added and stirring was continued until a white suspension was obtained. The inorganic salts were filtered off and extracted with several 200 ml portions of tetrahydrofuran (THF). The combined organic extracts were evaporated and distilled twice in vacuum to yield 50.23 g (66.5%) of the title compound. B.p. 116°-125° (0.02 mm Hg).

후처리

  1. temperatureto maintain a gentle reflux
  2. stirringstirring
  3. customwas obtained
  4. filtrationThe inorganic salts were filtered off
  5. extractionextracted with several 200 ml portions of tetrahydrofuran (THF)
  6. customThe combined organic extracts were evaporated
  7. distillationdistilled twice in vacuum

출처 및 근거

ORD 기록
ord-a734558324664f67a0840fe933ae2966
출처 데이터셋
uspto-grants-1989_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04798833

반응 노트

불러오는 중…