Hydrochloric Acid → HCID 22151847, compound

HRID 1194123Notes

Reaction equation

HRID 1194123 reaction equation
C[N:2]([CH3:7])[CH:3]=[CH:4][CH:5]=[O:6].Cl.[Cl:9][C:10]1[C:19]([Cl:20])=[CH:18][CH:17]=[CH:16][C:11]=1[C:12](=O)CN.CC[O-].[Na+].Cl>C(O)C>[CH:5]([C:4]1[C:12]([C:11]2[CH:16]=[CH:17][CH:18]=[C:19]([Cl:20])[C:10]=2[Cl:9])=[CH:7][NH:2][CH:3]=1)=[O:6]

Participants

6

Procedure

5.4 g of 3-dimethylaminoacrolein, 3.2 g of 2,3-dichlorophenacylamine hydrochloride and 60 ml of ethanol are heated for 11/2 hours under reflux. Then a solution of sodium ethylate in ethanol (prepared from 1 g of sodium and 15 ml of ethanol) is added dropwise and the reaction mixture is heated under reflux for another 30 minutes. After it has cooled to room temperature, the reaction mixture is poured into ice/water and neutralised with hydrochloric acid. The precipitate is washed with water, dried in vacuo, and the dry residue is purified by column chromatography (silica gel; elution with a 4:1 mixture of toluene/ethyl acetate). M.p. 152°-154° C. IR (solid/KBr) in cm-1 : 1655 (CO). 1H-NMR (CDCL3) in ppm: 7.0 (broad s, 1H); 7.3 (m, 2H); 9.66 (s, 1H); 11,9 (s, 1H, H replaceable with D2O). Mass peak at 204. This substance is novel, has fungicidal activity, and falls within the ambit of the invention.

Workup

  1. temperatureunder reflux
  2. temperaturethe reaction mixture is heated
  3. temperatureunder reflux for another 30 minutes
  4. washThe precipitate is washed with water
  5. customdried in vacuo
  6. customthe dry residue is purified by column chromatography (silica gel
  7. washelution
  8. additionwith a 4:1 mixture of toluene/ethyl acetate)

Sources & evidence

ORD record
ord-2b021589317a48ebb7470eb773ce9e7c
Source dataset
uspto-grants-1989_03
Patent number
US04812580

Reaction notes

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