Ethylenediamine → HCID 57548172, compound

HRID 1993905Notes

Reaction equation

HRID 1993905 reaction equation
C[Al](C)C.[CH2:5]([NH2:8])[CH2:6][NH2:7].C(O[C:12](=O)[CH2:13][O:14][C:15]1[CH:20]=[CH:19][C:18]([Cl:21])=[C:17]([F:22])[CH:16]=1)C>C1(C)C=CC=CC=1>[Cl:21][C:18]1[CH:19]=[CH:20][C:15]([O:14][CH2:13][C:12]2[NH:7][CH2:6][CH2:5][N:8]=2)=[CH:16][C:17]=1[F:22]

Participants

5

Procedure

To dry toluene (4 ml) under an inert atmosphere at 0° C. was added a toluene solution of trimethylaluminium (3.44 ml, 6.88 mmol, 2 M solution). A solution of ethylenediamine (0.46 ml, 6.88 mmol) in toluene (1.5 ml) was then added dropwise and the reaction mixture was then allowed to warm to room temperature and stirred for 1 h at this temperature before being re-cooled to 0° C. To this mixture was added dropwise a solution of (4-chloro-3-fluoro-phenoxy)-acetic acid ethyl ester (0.80 g, 3.44 mmol) in toluene (3 ml). The reaction mixture was then heated at 95° C. for 45 min and then cooled first to room temperature and finally to 0° C. The mixture was quenched by dropwise addition of methanol (1 ml) and when all gas evolution had ceased the mixture was diluted with water and extracted twice with ethyl acetate. The combined organic extracts were dried over sodium sulphate, filtered and concentrated in vacuo. The residue was triturated in ether to yield a white solid (0.73 g, 92%) which was collected by filtration; MS (ISP): 231.2, 229.3 ([M+H]+.).

Workup

  1. temperaturebefore being re-cooled to 0° C
  2. temperatureThe reaction mixture was then heated at 95° C. for 45 min
  3. temperaturecooled first to room temperature and finally to 0° C
  4. customThe mixture was quenched by dropwise addition of methanol (1 ml) and when all gas evolution
  5. additionwas diluted with water
  6. extractionextracted twice with ethyl acetate
  7. dry with materialThe combined organic extracts were dried over sodium sulphate
  8. filtrationfiltered
  9. concentrationconcentrated in vacuo
  10. customThe residue was triturated in ether

Sources & evidence

ORD record
ord-923d7ac6e59b46ebad1c781079ec32dc
Source dataset
uspto-grants-2010_01
Patent number
US07652055B2

Reaction notes

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