Acetic Acid → (+/-)-cis-6-(3,4-Dimethoxyphenyl)-cyclohex-3-enylamine

HRID 1050828Notes

Reaction equation

HRID 1050828 reaction equation
[CH3:1][O:2][C:3]1[CH:8]=[CH:7][C:6]([C@@H:9]2[CH2:14][CH:13]=[CH:12][CH2:11][C@@H:10]2[N+:15]([O-])=O)=[CH:5][C:4]=1[O:18][CH3:19].C(O)(=O)C>C(O)C.[Zn]>[CH3:19][O:18][C:4]1[CH:5]=[C:6]([C@@H:9]2[C@H:10]([NH2:15])[CH2:11][CH:12]=[CH:13][CH2:14]2)[CH:7]=[CH:8][C:3]=1[O:2][CH3:1]

Participants

5

Procedure

40 g of (±)-cis-1,2-dimethoxy-4-(2-nitrocyclohex-4-enyl)benzene (compound F7) are dissolved in 400 ml of ethanol and 40 g of zinc powder are added. After heating to boiling temperature, 65 ml of glacial acetic acid are added dropwise. Afterwards, the reaction mixture is filtrated and concentrated. The residue is redissolved in diluted hydrochloric acid and extracted with toluene. The aqueous layer is alkalized using 6 N solution of sodium hydroxide and extracted several times with toluene. The combined organic phases of the alkalic extraction are dried using sodium sulfate and concentrated. The residue is chromatographed on silica gel. 11.5 g of the title compound are obtained.

Workup

  1. temperatureAfter heating
  2. additionare added dropwise
  3. filtrationAfterwards, the reaction mixture is filtrated
  4. concentrationconcentrated
  5. dissolutionThe residue is redissolved in diluted hydrochloric acid
  6. extractionextracted with toluene
  7. extractionextracted several times with toluene
  8. extractionThe combined organic phases of the alkalic extraction
  9. customare dried
  10. concentrationconcentrated
  11. customThe residue is chromatographed on silica gel

Sources & evidence

ORD record
ord-f32dd24680144cb3b8e0c7555294939e
Source dataset
uspto-grants-2016_07
Patent number
US09387205B2

Reaction notes

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