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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Trichloroisocyanuric Acid → HCID 20544433, 화합물

HRID 2285842
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HRID 2285842 반응식
[O:1]=[C:2]1[CH:7]=[C:6]([CH2:8][OH:9])[NH:5][CH:4]=[C:3]1[O:10][CH2:11][C:12]([OH:14])=[O:13].[Cl:15]N1C(=O)N(Cl)C(=O)N(Cl)C1=O>CO.O>[O:1]=[C:2]1[C:7]([Cl:15])=[C:6]([CH2:8][OH:9])[NH:5][CH:4]=[C:3]1[O:10][CH2:11][C:12]([OH:14])=[O:13]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 6909Trichloroisocyanuric AcidHCID 20544454HCID 20544454, 화합물

생성물 1

HCID 20544433HCID 20544433, 화합물수율 121.2%

시약·촉매·용매 2

HCID 887Methanol용매HCID 962Water용매

실험 절차

2-(4-Oxo-6-hydroxymethyl-1,4-dihydropyridin-3-yloxy)acetic acid (5.97 g) was dissolved in a mixture of methanol (300 ml) and water (420 ml) at 65° to 70° C. and the solution was stirred at the same temperature. Trichloroisocyanuric acid (2.79 g) was added thereto, and the resultant mixture was stirred at the same temperature for 1.5 hours and then allowed to stand at room temperature over-night. The reaction mixture was cooled and the resulting crystals were collected by filtration, washed with water and dried. Thus obtained crystals (4.1 g) were recrystallized from water (100 ml) to give crystals (3.4 g) of 2-(4-oxo-5-chloro-6-hydroxymethyl-1,4-dihydropyridin-3-yloxy) acetic acid, mp 240° to 245° C.(dec).

후처리

  1. waitto stand at room temperature over-night
  2. temperatureThe reaction mixture was cooled
  3. filtrationthe resulting crystals were collected by filtration
  4. washwashed with water
  5. customdried
  6. customThus obtained crystals (4.1 g) were recrystallized from water (100 ml)

출처 및 근거

ORD 기록
ord-0bed78c286184b4ca7b48398e83d44fd
출처 데이터셋
uspto-grants-1982_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04324892

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