2-Chloro-N,N-dimethylethylamine → HCID 85439121, compound

HRID 442028Notes

Reaction equation

HRID 442028 reaction equation
[Cl:1][CH2:2][CH2:3][N:4]([CH3:6])[CH3:5].[Na].[Cl:8][C:9]1[CH:22]=[CH:21][C:12]([C:13](=[N:15][O:16][CH2:17][C:18]([OH:20])=[O:19])[CH3:14])=[CH:11][CH:10]=1>CN(C)C=O.O>[ClH:1].[CH3:5][N:4]([CH3:6])[CH2:3][CH2:2][O:20][C:18](=[O:19])[CH2:17][O:16][N:15]=[C:13]([CH3:14])[C:12]1[CH:21]=[CH:22][C:9]([Cl:8])=[CH:10][CH:11]=1

Participants

6

Procedure

4.3 g of 2-chloro-N,N-dimethyl ethylamine was added to a suspension of 10 g of the sodium salt of (4-chloro-α -methylbenzylidene)amino-oxyacetic acid in 30 ml of dimethylformamide. The mixture was stirred for 72 hours. It was then diluted with water and extracted with diethylether. The resulting ethereal solution was extracted with 20 ml of 2N hydrochloric acid. The acid extract was then made basic with 30ml of 2N sodium hydroxide and extracted with diethylether. The latter ethereal extract was washed, dried over anhydrous sodium sulphate and after concentration by evaporation neutralized with alcoholic hydrochloric acid. When diethylether was added the hydrochloride of the (2-dimethyl-aminoethyl)ester of (4-chloro-α -methylbenzylidene) aminooxyacetic acid crystallized out. It was recrystallized from an alcohol-ether mixture; melting point 160° -162° C with decomposition.

Workup

  1. extractionextracted with diethylether
  2. extractionThe resulting ethereal solution was extracted with 20 ml of 2N hydrochloric acid
  3. extractionThe acid extract
  4. extractionextracted with diethylether
  5. extractionThe latter ethereal extract
  6. washwas washed
  7. dry with materialdried over anhydrous sodium sulphate
  8. concentrationafter concentration
  9. customby evaporation
  10. additionWhen diethylether was added the hydrochloride of the (2-dimethyl-aminoethyl)ester of (4-chloro-α -methylbenzylidene) aminooxyacetic acid
  11. customcrystallized out
  12. customIt was recrystallized from an alcohol-ether mixture

Sources & evidence

ORD record
ord-d7024198808444cca8cf9a8917e129a7
Source dataset
uspto-grants-1977_08
Patent number
US04044023

Reaction notes

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