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Phenol → 2-Chloro-4,6-diphenoxy-1,3,5-triazine

HRID 1390100
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HRID 1390100 반응식
[N:1]1[C:8]([Cl:9])=[N:7][C:5](Cl)=[N:4][C:2]=1Cl.[C:10]1([OH:16])[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1.[OH-:17].[Na+]>CC(C)=O.O>[O:16]([C:2]1[N:4]=[C:5]([O:17][C:10]2[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=2)[N:7]=[C:8]([Cl:9])[N:1]=1)[C:10]1[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

HCID 996PhenolHCID 7954Cyanuric chlorideHCID 14798Sodium Hydroxide

생성물 1

HCID 180882-Chloro-4,6-diphenoxy-1,3,5-triazine수율 82.4%

시약·촉매·용매 2

HCID 180Acetone용매HCID 962Water용매

실험 절차

To a solution of 18.4 g (0.1 mole) of cyanuric chloride in 90 ml of acetone was added dropwise a solution of 19.0 g (0.2 moles) of phenol and 8.0 g (0.2 moles) of sodium hydroxide in 75 ml of water at a reaction temperature in the range of 15° to 20° C. After 41/2 hours the precipitate formed was removed by suction, washed with water and dried (with Mg SO4). Purification by recrystallization from n-heptane gave 24.7 g of 2,4-diphenoxy-6-chloro-s-triazine in 82% yield. The melting point was 119°-121° C.

후처리

  1. customAfter 41/2 hours the precipitate formed
  2. customwas removed by suction
  3. washwashed with water
  4. dry with materialdried (with Mg SO4)
  5. customPurification
  6. customby recrystallization from n-heptane

출처 및 근거

ORD 기록
ord-1395c42c2e4d4a1a976bf98bbb3eeedc
출처 데이터셋
uspto-grants-1981_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04247692

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