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Stannous chloride dihydrate → 3-Chloro-4-ethylaniline

HRID 1857431
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HRID 1857431 반응식
[Cl:1][C:2]1[CH:3]=[C:4]([N+:10]([O-])=O)[CH:5]=[CH:6][C:7]=1[CH2:8][CH3:9].O.O.Cl[Sn]Cl>>[Cl:1][C:2]1[CH:3]=[C:4]([CH:5]=[CH:6][C:7]=1[CH2:8][CH3:9])[NH2:10]
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참가 물질

3

반응물 2

HCID 61436Stannous chloride dihydrateHCID 41134491-Chloro-2-ethyl-5-nitrobenzene

생성물 1

HCID 211899483-Chloro-4-ethylaniline수율 98%

실험 절차

A solution of 8.9 g (48 mmol) of 31 and 54.6 g (241 mmol) of SnCl2.2H2O in 100 mL of absolute alcohol was refluxed for 1 h. It was evaporated to remove most of the solvent and the residue was treated with 2N NaOH to pH=9. The mixture was filtered and the solid was washed with methanol (10 mL) and ethyl acetate (200 mL). The filtrate was separated and the aqueous phase was extracted with ethyl acetate (2×50 mL). The combined organic solution was dried (MgSO4) and evaporated to leave 7.31 g (98%) of liquid. 1H NMR (CDCl3), 1.178 (t, 3, J=7.5), 2.639 (q, 2, J=7.4), 6.532 (dd, 1, J=2.2, 8.1), 6.700 (d, 1, J=2.2), 6.996 (d, 1, J=8.2).

후처리

  1. customIt was evaporated
  2. customto remove most of the solvent
  3. additionthe residue was treated with 2N NaOH to pH=9
  4. filtrationThe mixture was filtered
  5. washthe solid was washed with methanol (10 mL) and ethyl acetate (200 mL)
  6. customThe filtrate was separated
  7. extractionthe aqueous phase was extracted with ethyl acetate (2×50 mL)
  8. dry with materialThe combined organic solution was dried (MgSO4)
  9. customevaporated

출처 및 근거

ORD 기록
ord-1b898e2fbfe345118ecef498e6157780
출처 데이터셋
uspto-grants-2000_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06147075

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