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Sodium Hydroxide → 4-(Methylsulfonyl)-3-(trifluoromethyl)phenylhydrazine hydrochloride

HRID 2086688
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HRID 2086688 반응식
[CH3:1][S:2]([C:5]1[CH:11]=[CH:10][C:8]([NH2:9])=[CH:7][C:6]=1[C:12]([F:15])([F:14])[F:13])(=[O:4])=[O:3].[N+:16]([O-])([O-])=O.[Na+].O.O.[Sn](Cl)[Cl:24].[OH-].[Na+]>Cl.O>[ClH:24].[CH3:1][S:2]([C:5]1[CH:11]=[CH:10][C:8]([NH:9][NH2:16])=[CH:7][C:6]=1[C:12]([F:13])([F:14])[F:15])(=[O:4])=[O:3]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 4

HCID 14798Sodium HydroxideHCID 24268Sodium NitrateHCID 61436Stannous chloride dihydrateHCID 223166824-(Methylsulfonyl)-3-(trifluoromethyl)aniline

생성물 1

HCID 223168444-(Methylsulfonyl)-3-(trifluoromethyl)phenylhydrazine hydrochloride수율 79.1%

시약·촉매·용매 2

HCID 313
Hydrochloric Acid
용매
2회
HCID 962Water용매

실험 절차

To a stirred suspension of 4-(methylsulfonyl)-3-(trifluoromethyl)aniline (1.04 g, 4.35 mmol) in conc. HCl (10 mL) was added dropwise a solution of sodium nitrate (0.315 g, 4.57 mmol) in water (10 mL) at −20° C. After stirring for 30 minutes, the resulting suspension was added Tin(II) chloride dihydrate (4.92 g, 21.8 mmol) in conc.HCl (10 mL) at −10° C. After stirring for 1 hour at −5° C., the mixture was stirred further 1 hour at room temperature. The reaction mixture was made alkaline with aqueous NaOH at 0-5° C. The mixture was filtered through Celite, the filterate was extracted with THF (30 mL×3), the combined organic layer washed with brine, dried over MgSO4 and concentration in vacuo to give the subtitle compound (1 g).

후처리

  1. customat −10° C
  2. stirringAfter stirring for 1 hour at −5° C.
  3. stirringthe mixture was stirred further 1 hour at room temperature
  4. customat 0-5° C
  5. filtrationThe mixture was filtered through Celite
  6. extractionthe filterate was extracted with THF (30 mL×3)
  7. washthe combined organic layer washed with brine
  8. dry with materialdried over MgSO4 and concentration in vacuo

출처 및 근거

ORD 기록
ord-90e26e6b4b4a4f9a87b12585cfa80f49
출처 데이터셋
uspto-grants-2004_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06727238B2

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