2-Nitro-4'-chloro diphenyl sulfide → 2-[(4-Chlorophenyl)sulfanyl]aniline

HRID 2185931노트

반응식

HRID 2185931 반응식
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([S:8][C:9]2[CH:14]=[CH:13][CH:12]=[CH:11][C:10]=2[N+:15]([O-])=O)=[CH:4][CH:3]=1.[Sn]>C(O)(=O)C.Cl>[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([S:8][C:9]2[CH:14]=[CH:13][CH:12]=[CH:11][C:10]=2[NH2:15])=[CH:6][CH:7]=1

참가 물질

5

반응물 2

HCID 3653942-Nitro-4'-chloro diphenyl sulfideHCID 5352426Tin atom

생성물 1

HCID 3612972-[(4-Chlorophenyl)sulfanyl]aniline수율 99.2%

시약·촉매·용매 2

HCID 176Acetic Acid용매HCID 313Hydrochloric Acid용매

실험 절차

2-(4-Chlorophenylthio)nitrobenzene (1.0 g) was dissolved in a mixture of acetic acid (5 ml) and 6N hydrochloride (5 ml), and tin (1.0 g) was added thereto, followed by stirring for six hours at room temperature. After the solvent was removed under reduced pressure, the residue was dissolved in water (50 ml) and a pH of the resultant solution was adjusted to 9-10 with potassium carbonate. The thus-obtained solution was extracted with ethyl acetate. The extracted solution was washed sequentially with water and saturated brine and dried over anhydrous sodium sulfate. Subsequently, the solvent was removed under reduced pressure and the residue was crystallized from ethyl acetate under stirring, to thereby yield the target compound (880 mg) as pale-yellow crystals.

후처리

  1. additionwas added
  2. customAfter the solvent was removed under reduced pressure
  3. dissolutionthe residue was dissolved in water (50 ml)
  4. extractionThe thus-obtained solution was extracted with ethyl acetate
  5. washThe extracted solution was washed sequentially with water and saturated brine
  6. dry with materialdried over anhydrous sodium sulfate
  7. customSubsequently, the solvent was removed under reduced pressure
  8. customthe residue was crystallized from ethyl acetate
  9. stirringunder stirring

출처 및 근거

ORD 기록
ord-6cfb0af81ac04dfa86555dec623ce70a
출처 데이터셋
uspto-grants-2002_06
특허 번호
US06403607B1

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