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Urea → 5-(4-Phenoxyphenyl)-1,3-diazinane-2,4,6-trione

HRID 1249680
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HRID 1249680 반응식
[O-:1][CH2:2]C.[Na+].[O:5]([C:12]1[CH:17]=[CH:16][C:15]([CH2:18][C:19]([O:21]CC)=O)=[CH:14][CH:13]=1)[C:6]1[CH:11]=[CH:10][CH:9]=[CH:8][CH:7]=1.[NH2:24][C:25]([NH2:27])=[O:26]>C(O)C>[O:5]([C:12]1[CH:13]=[CH:14][C:15]([CH:18]2[C:19](=[O:21])[NH:27][C:25](=[O:26])[NH:24][C:2]2=[O:1])=[CH:16][CH:17]=1)[C:6]1[CH:7]=[CH:8][CH:9]=[CH:10][CH:11]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 1176UreaHCID 2723922Sodium ethoxideHCID 13567666Ethyl 2-(4-phenoxyphenyl)acetate

생성물 1

HCID 116737785-(4-Phenoxyphenyl)-1,3-diazinane-2,4,6-trione수율 21.7%

시약·촉매·용매 1

HCID 702Ethanol용매2회

실험 절차

A solution of sodium ethoxide (0.27 g) in 3 ml of anhydrous ethanol is added with 0.657 g of ethyl (4′-phenoxyphenyl)acetate dissolved in 5 ml of ethanol, then with urea (0.18 g). The reaction mixture is refluxed for 2 hours 30 minutes, then it is cooled to room temperature and the suspended solid is filtered. The solid is redissolved in 8 ml of water and the solution is acidified with 1 N hydrochloric acid. The solid which separates is recovered by filtration to give 0.165 g of the product. m.p.>240° C.

후처리

  1. temperatureThe reaction mixture is refluxed for 2 hours 30 minutes
  2. filtrationthe suspended solid is filtered
  3. dissolutionThe solid is redissolved in 8 ml of water
  4. filtrationThe solid which separates is recovered by filtration

출처 및 근거

ORD 기록
ord-8296e46121bc4e0dbee55d87b2353fbb
출처 데이터셋
uspto-grants-2002_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06335332B1

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