Ethanolamine → HCID 20278973, compound

HRID 1156339Notes

Reaction equation

HRID 1156339 reaction equation
[C:1]([C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][C:5]=1[NH:10][C:11](=[O:16])[C:12]([Cl:15])([Cl:14])[Cl:13])(=O)[CH3:2].[NH2:17][CH2:18][CH2:19][OH:20]>C(O)C>[Cl:13][C:12]([Cl:15])([Cl:14])[C:11]([NH:10][C:5]1[CH:6]=[CH:7][CH:8]=[CH:9][C:4]=1[C:1](=[N:17][CH2:18][CH2:19][OH:20])[CH3:2])=[O:16]

Participants

4

Procedure

A mixture of 60 parts of N-(2-acetylphenyl)-2,2,2-trichloroacetamide, 14 parts of 2-aminoethanol and 200 parts of ethanol is stirred first for 5.50 hours at reflux and further overnight while the temperature is allowed to cool to room temperature. The formed precipitate is filtered off. The product is washed with 2,2'-oxybispropane and dried in vacuo, yielding 40 parts (59%) of 2,2,2-trichloro-N-[2-[1-[(2-hydroxyethyl)imino]ethyl]phenyl]acetamide; mp. 182° C.

Workup

  1. temperatureat reflux and further overnight while the temperature
  2. filtrationThe formed precipitate is filtered off
  3. washThe product is washed with 2,2'-oxybispropane
  4. customdried in vacuo

Sources & evidence

ORD record
ord-d864191d968845c6997f4cc5b2fc93f2
Source dataset
uspto-grants-1982_06
Patent number
US04335127

Reaction notes

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