Ethanol → HCID 61718883, compound

HRID 575732Notes

Reaction equation

HRID 575732 reaction equation
[Br:1][C:2]1[CH:7]=[C:6]([N+:8]([O-])=O)[CH:5]=[CH:4][C:3]=1[O:11][CH2:12][CH:13]1[CH2:15][CH2:14]1.[Cl-].[NH4+].O.C(O)C>C1COCC1.[Fe]>[Br:1][C:2]1[CH:7]=[C:6]([CH:5]=[CH:4][C:3]=1[O:11][CH2:12][CH:13]1[CH2:14][CH2:15]1)[NH2:8]

Participants

7

Procedure

A mixture of 2-bromo-1-(cyclopropylmethoxy)-4-nitrobenzene (1.07 g, 3.9 mmol), ammonium chloride (421 mg, 7.8 mmol), and iron powder (1.1 g, 20 mmol) suspended in THF (6.5 mL), water (2.5 mL) and ethanol (6.5 mL) was heated to 95° C. using microwave irradiation (normal) for 3 h. The crude reaction mixture was filtered through a short plug of celite; the celite plug was washed with MeOH (˜10 mL). The resulting filtrate was concentrated in vacuo. The resulting residue was diluted with EtOAc (50 ml) and washed with saturated bicarbonate solution (aq), dried over anhydrous magnesium sulfate, filtered, and concentrated in vacuo to afford the title compound, (939 mg, 90%). The material was carried forward without any further purification. LCMS (M+H)+=242.

Workup

  1. custommicrowave irradiation (normal) for 3 h
  2. customThe crude reaction mixture
  3. filtrationwas filtered through a short plug of celite
  4. washthe celite plug was washed with MeOH (˜10 mL)
  5. concentrationThe resulting filtrate was concentrated in vacuo
  6. additionThe resulting residue was diluted with EtOAc (50 ml)
  7. washwashed with saturated bicarbonate solution (aq)
  8. dry with materialdried over anhydrous magnesium sulfate
  9. filtrationfiltered
  10. concentrationconcentrated in vacuo

Sources & evidence

ORD record
ord-9b3b24bfc8de48d1a362102d9b8df6f3
Source dataset
uspto-grants-2015_05
Patent number
US09034900B2

Reaction notes

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