Hydrochloric Acid → 3-Chloro-4-morpholinoaniline

HRID 56228

Reaction equation

HRID 56228 reaction equation
Cl.O.[Cl:3][C:4]1[CH:9]=[C:8]([N+:10]([O-])=O)[CH:7]=[CH:6][C:5]=1[N:13]1[CH2:18][CH2:17][O:16][CH2:15][CH2:14]1.CCN(CC)CC>CO.[Fe]>[Cl:3][C:4]1[CH:9]=[C:8]([CH:7]=[CH:6][C:5]=1[N:13]1[CH2:18][CH2:17][O:16][CH2:15][CH2:14]1)[NH2:10]

Participants

7

Conditions

Temperature
65 °C

Procedure

To a mixture of concentrated hydrochloric acid (1.0 mL) and water (50 mL) was added iron powder (7.55 g, 135 mmol) in one portion and the mixture was stirred at 65° C. for 15 min. The aqueous layer of the mixture was poured out and a solution of 4-(2-chloro-4-nitrophenyl)morpholine (3.28 g, 13.5 mmol) in MeOH (50 mL) was added to the above processed iron powder. The mixture was acidified to pH 3 with hydrochloric acid and stirred further at 65° C. for 45 min. The mixture was then cooled to rt, adjusted to pH 10 with Et3N and filtered and the filtrate was concentrated in vacuo. The residue was dissolved in DCM (150 mL) and the solution was washed with water (100 mL×3) and brine (100 mL), dried over anhydrous Na2SO4 and concentrated in vacuo to give the title compound as a white solid (2.05 g, 71%).

Workup

  1. additionThe aqueous layer of the mixture was poured out
  2. stirringstirred further at 65° C. for 45 min
  3. temperatureThe mixture was then cooled to rt
  4. filtrationfiltered
  5. concentrationthe filtrate was concentrated in vacuo
  6. dissolutionThe residue was dissolved in DCM (150 mL)
  7. washthe solution was washed with water (100 mL×3) and brine (100 mL)
  8. dry with materialdried over anhydrous Na2SO4
  9. concentrationconcentrated in vacuo

Sources & evidence

ORD record
ord-06b1569164fa437880b489155b479a9c
Source dataset
uspto-grants-2016_09
Patent number
US09434695B2

Linked notes

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