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Hydrochloric Acid → 2-Chloro-6-(4,6-dimethoxytriazin-2-yloxy)-benzoic acid

HRID 345269
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HRID 345269 반응식
CC([O-])(C)C.[K+].[Cl:7][C:8]1[CH:16]=[CH:15][CH:14]=[C:13]([OH:17])[C:9]=1[C:10]([OH:12])=[O:11].Cl[N:19]1[N:24]=[C:23]([O:25][CH3:26])[CH:22]=[C:21]([O:27][CH3:28])[NH:20]1.Cl>CN(C)C=O.O>[Cl:7][C:8]1[CH:16]=[CH:15][CH:14]=[C:13]([O:17][N:19]2[N:20]=[C:21]([O:27][CH3:28])[CH:22]=[C:23]([O:25][CH3:26])[NH:24]2)[C:9]=1[C:10]([OH:12])=[O:11]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 4

HCID 313Hydrochloric AcidHCID 925912-Chloro-6-hydroxybenzoic acidHCID 221477162-Chloro-4,6-dimethoxy-triazineHCID 23665647Potassium tert-butoxide

생성물 1

HCID 199918532-Chloro-6-(4,6-dimethoxytriazin-2-yloxy)-benzoic acid

시약·촉매·용매 2

HCID 962Water용매
HCID 6228Dimethylformamide용매

반응 조건

온도
25 °C

실험 절차

At 25° C., 20.2 g of potassium tert-butylate is added in portions to 15.5 g of 2-chloro-6-hydroxybenzoic acid in 50 ml of dimethylformamide. Subsequently, 15.7 g of 2-chloro-4,6-dimethoxytriazine is added. The mixture is stirred for 12 hours at 25° C. and poured into cold water, and the resulting mixture is acidified with hydrochloric acid. Extraction is then carried out with ethyl acetate, and the extract is dried over sodium sulfate and the solvent is removed under reduced pressure. The residue is stirred with a small amount of diethyl ether, followed by filtration. The residue is dried under reduced pressure (m.p. 128°-131° C.).

후처리

  1. extractionExtraction
  2. dry with materialthe extract is dried over sodium sulfate
  3. customthe solvent is removed under reduced pressure
  4. stirringThe residue is stirred with a small amount of diethyl ether
  5. filtrationfollowed by filtration
  6. customThe residue is dried under reduced pressure (m.p. 128°-131° C.)

출처 및 근거

ORD 기록
ord-9f0396cf4ca84c5d8c905f274e7561e5
출처 데이터셋
uspto-grants-1991_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05057143

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