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Hydrochloric Acid → 2-Iodo-5-methylbenzoic acid

HRID 372415
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인쇄 미리보기

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HRID 372415 반응식
[CH3:1][C:2]1[CH:10]=[C:6]([C:7]([OH:9])=[O:8])[C:5](N)=[CH:4][CH:3]=1.Cl.N([O-])=O.[Na+].[I-:17].[K+].S([O-])([O-])(=O)=S.[Na+].[Na+]>O>[I:17][C:5]1[CH:4]=[CH:3][C:2]([CH3:1])=[CH:10][C:6]=1[C:7]([OH:9])=[O:8]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 5

HCID 313Hydrochloric Acid2회HCID 4875Potassium IodideHCID 24477Sodium ThiosulfateHCID 762552-Amino-5-methylbenzoic acidHCID 23668193Sodium Nitrite

생성물 1

HCID 1429412-Iodo-5-methylbenzoic acid

시약·촉매·용매 1

HCID 962
Water
용매
2회

실험 절차

20 G. of 5-methyl-anthranilic acid are suspended in 200 ml. of 3-N hydrochloric acid at 0° C. A solution of 10 g. of sodium nitrite and 20 ml. of water is added dropwise thereto with stirring and the mixture is further stirred for 25 minutes at 0° C. A solution of 26.5 g. of potassium iodide, 30 ml. of 3-N hydrochloric acid and 30 ml. of water is then added dropwise at 5°-10° C. The mixture is stirred for an additional 30 minutes at room temperature and for 2 hours at reflux. The mixture is cooled and sodium thiosulfate is added until the solution is yellow (5 g.). The crystalline 2-iodo-5-methyl-benzoic acid obtained is removed by filtration under vacuum and washed neutral with water. The crude acid is dissolved in ether, washed well with sodium thiosulfate solution and water, dried over sodium sulfate and evaporated, and there are obtained light-brown crystals having a melting point of 100°-112° C.

후처리

  1. customat 0° C
  2. stirringthe mixture is further stirred for 25 minutes at 0° C
  3. stirringThe mixture is stirred for an additional 30 minutes at room temperature and for 2 hours
  4. temperatureat reflux
  5. temperatureThe mixture is cooled

출처 및 근거

ORD 기록
ord-8584c24911694cf396e0ddab66dc7209
출처 데이터셋
uspto-grants-1978_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04091023

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