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Ethylenediamine → HCID 57548152, compound

HRID 1993907
Notes
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Reaction equation

HRID 1993907 reaction equation
C[Al](C)C.[CH2:5]([NH2:8])[CH2:6][NH2:7].C(O[C:12](=O)[CH2:13][S:14][C:15]1[CH:20]=[C:19]([Cl:21])[CH:18]=[C:17]([Cl:22])[CH:16]=1)C>C1(C)C=CC=CC=1>[Cl:22][C:17]1[CH:16]=[C:15]([S:14][CH2:13][C:12]2[NH:7][CH2:6][CH2:5][N:8]=2)[CH:20]=[C:19]([Cl:21])[CH:18]=1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

5

Reactant 3

HCID 3301EthylenediamineHCID 16682925TrimethylaluminumHCID 68537666Ethyl 2-[(3,5-dichlorophenyl)thio]acetate

Product 1

HCID 57548152HCID 57548152, compoundYield 30%

Reagents, catalysts & solvents 1

HCID 1140TolueneSolvent4×

Procedure

To dry toluene (4 ml) under an inert atmosphere at 0° C. was added a toluene solution of trimethylaluminium (2.70 ml, 5.39 mmol, 2 M solution). A solution of ethylenediamine (0.36 ml, 5.39 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 (3,5-dichloro-phenylsulfanyl)-acetic acid ethyl ester (0.72 g, 2.70 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 (0.21 g, 30%) which was collected by filtration; MS (ISP): 265.0, 263.1, 261.1 ([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-b70c3fe9c9624e75ba9a3aa559c84357
Source dataset
uspto-grants-2010_01
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US07652055B2

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes