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Water → HCID 20553700, 화합물

HRID 1106232
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HRID 1106232 반응식
[F:1][C:2]1[CH:3]=[C:4]([NH2:15])[C:5](=[CH:9][C:10]=1[S:11](=[O:14])(=[O:13])[NH2:12])[C:6]([OH:8])=[O:7].O.[C:17](=O)([O-])[O-].[K+].[K+]>CO.S(=O)(=O)(O)O>[NH2:15][C:4]1[CH:3]=[C:2]([F:1])[C:10]([S:11](=[O:13])(=[O:14])[NH2:12])=[CH:9][C:5]=1[C:6]([O:8][CH3:17])=[O:7]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

HCID 962WaterHCID 11430Potassium CarbonateHCID 205536982-AMINO-5-(AMINOSULFONYL)-4-FLUOROBENZOIC ACID

생성물 1

HCID 20553700HCID 20553700, 화합물

시약·촉매·용매 2

HCID 887Methanol용매2회HCID 1118Sulfuric Acid용매

실험 절차

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트

A reaction flask, containing 7.2 g (0.0307 molecule) of 4-fluoro-5-sulphamylanthranilic acid (6) in 125 ml of methanol and 10 ml of concentrated sulphuric acid, was attached to a Soxhlet apparatus, containing molecular sieves 4A, immersed in methanol (25 ml). After 48 hours' reflux, the solution was poured into cold water (500 ml), containing 25 g of potassium carbonate. The solid, which separated out, was recovered on a filter and dried in vacuo at 80°; yield: 5.6 g (73.7%); m.p.: 209°-211°.

후처리

  1. temperatureAfter 48 hours' reflux
  2. customThe solid, which separated out
  3. customwas recovered on
  4. filtrationa filter
  5. customdried in vacuo at 80°

출처 및 근거

ORD 기록
ord-b8499628158a4cf09f10c013b10b43d7
출처 데이터셋
uspto-grants-1982_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04312862

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