2-[2-[(2-Nitrophenyl)methyl]3-thienyl]-1,3-dioxolane → 4,10-Dihydro-5H-thieno[3,2-c][1]benzazepine

HRID 1938251Notes

Reaction equation

HRID 1938251 reaction equation
[N+:1]([C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][C:5]=1[CH2:10][C:11]1[S:12][CH:13]=[CH:14][C:15]=1[CH:16]1OCCO1)([O-])=O>CC(C)=O.C(O)(=O)C.[Zn]>[S:12]1[C:11]2[CH2:10][C:5]3[CH:6]=[CH:7][CH:8]=[CH:9][C:4]=3[NH:1][CH2:16][C:15]=2[CH:14]=[CH:13]1

Participants

5

Reactant 1

HCID 111300652-[2-[(2-Nitrophenyl)methyl]3-thienyl]-1,3-dioxolane

Product 1

HCID 108673664,10-Dihydro-5H-thieno[3,2-c][1]benzazepineYield 72.4%

Reagents, catalysts & solvents 3

HCID 23994ZincCatalystHCID 176Acetic AcidSolventHCID 180AcetoneSolvent

Procedure

A stirred solution of 4 gms of 2-[2-[(2-nitrophenyl)methyl]-3-thienyl]-1,3-dioxolane in acetone (50 ml) and acetic acid (90% 50 ml) is heated to 60° C. Zinc dust (10 gms) is slowly added and after the addition, reaction mixture is stirred for 6 hours. At the end, reaction mixture is filtered and the residue washed with acetone and concentrated. The brown residue is extracted with chloroform and washed well with water. The organic layer is dried (Na2SO4) and filtered and concentrated. The product is isolated by silica gel column chromatography by eluting with 20% ethyl acetate:hexane to give 2.0 g of the desired product as a pale yellow crystalline solid, m.p. 86° C. Mass Spectrum; M+ 202.

Workup

  1. additionafter the addition, reaction mixture
  2. customAt the end, reaction mixture
  3. filtrationis filtered
  4. washthe residue washed with acetone
  5. concentrationconcentrated
  6. extractionThe brown residue is extracted with chloroform
  7. washwashed well with water
  8. dry with materialThe organic layer is dried (Na2SO4)
  9. filtrationfiltered
  10. concentrationconcentrated
  11. customThe product is isolated by silica gel column chromatography
  12. washby eluting with 20% ethyl acetate

Sources & evidence

ORD record
ord-6a7a2af910a94ba1a96a2bd28dba891a
Source dataset
uspto-grants-1997_12
Patent number
US05693635

Reaction notes

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