Water → HCID 18543578, compound

HRID 1249872Notes

Reaction equation

HRID 1249872 reaction equation
Cl[CH2:2][C:3]([NH:5][C:6]1[CH:11]=[CH:10][C:9]([N+:12]([O-:14])=[O:13])=[CH:8][C:7]=1[Cl:15])=[O:4].C(=O)([O-])[O-].[Na+].[Na+].Cl.[CH3:23][N:24]([CH3:28])[CH2:25][CH2:26][SH:27].O>CN(C)C=O>[Cl:15][C:7]1[CH:8]=[C:9]([N+:12]([O-:14])=[O:13])[CH:10]=[CH:11][C:6]=1[NH:5][C:3](=[O:4])[CH2:2][S:27][CH2:26][CH2:25][N:24]([CH3:28])[CH3:23]

Participants

6

Conditions

Temperature
25 °C

Procedure

To a solution of N-(chloroacetyl)-2-chloro-4-nitroaniline (3.01 g) in N,N-dimethylformamide (100 mL) is added powdered sodium carbonate (6.0 g) and 2-dimethylaminoethanethiol hydrochloride (6.0 g). The mixture is stirred for 1 hour at 25° C., poured into water and extracted into ethyl acetate. The ethyl acetate solution is dried over anhydrous potassium carbonate and concentrated under reduced pressure to give an oil. The oil is crystallized from toluene-hexanes (3:1) to yield a pale yellow crystalline solid.

Workup

  1. extractionextracted into ethyl acetate
  2. dry with materialThe ethyl acetate solution is dried over anhydrous potassium carbonate
  3. concentrationconcentrated under reduced pressure
  4. customto give an oil
  5. customThe oil is crystallized from toluene-hexanes (3:1)
  6. customto yield a pale yellow crystalline solid

Sources & evidence

ORD record
ord-a579e19f8b8441bc83d5562823b5a418
Source dataset
uspto-grants-2002_01
Patent number
US06335350B1

Reaction notes

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