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Ethylene Glycol → HCID 19370278, 화합물

HRID 129735
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HRID 129735 반응식
C(OC([N:6]1[CH2:11][CH2:10][N:9]([CH2:12][CH2:13][O:14][C:15]([C:23]2[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=2)([C:17]2[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=2)[CH3:16])[CH2:8][CH2:7]1)=O)C.[OH-].[K+].C(O)CO>O>[C:23]1([C:15]([C:17]2[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=2)([O:14][CH2:13][CH2:12][N:9]2[CH2:8][CH2:7][NH:6][CH2:11][CH2:10]2)[CH3:16])[CH:24]=[CH:25][CH:26]=[CH:27][CH:28]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 174Ethylene GlycolHCID 14797Potassium HydroxideHCID 19370330HCID 19370330, 화합물

생성물 1

HCID 19370278HCID 19370278, 화합물수율 71.1%

시약·촉매·용매 1

HCID 962Water용매2회

실험 절차

A mixture of 2.6 g (6.8 mmole) of 4-ethoxycarbonyl-1-[2-(1,1-diphenylethoxy)ethyl]piperazine [prepared as described in step (a) above], 3.0 g (5.3 mmole) of potassium hydroxide, 9 ml of water and 30 ml of ethylene glycol was stirred at 160° C. for 2 hours while the water formed was removed by evaporation. The reaction mixture was then poured into ice water, and the mixture was extracted with chloroform, after which it was washed with water. The solvent was then removed by evaporation under reduced pressure, to obtain 1.5 g (yield 71%) of the title compound as an oil.

후처리

  1. customformed
  2. customwas removed by evaporation
  3. additionThe reaction mixture was then poured into ice water
  4. extractionthe mixture was extracted with chloroform
  5. washafter which it was washed with water
  6. customThe solvent was then removed by evaporation under reduced pressure

출처 및 근거

ORD 기록
ord-7267fbd517574729a74c9ea98392fb60
출처 데이터셋
uspto-grants-1995_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05470851

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