2-Chloropropionic acid → HCID 18316267, compound

HRID 276678Notes

Reaction equation

HRID 276678 reaction equation
[CH3:1][C:2]1[CH:7]=[C:6]([N+:8]([O-:10])=[O:9])[CH:5]=[CH:4][C:3]=1[N:11]=[C:12]=[S:13].[CH2:14]([CH:16]([CH2:19][CH3:20])[CH2:17][NH2:18])[CH3:15].Cl[CH:22]([CH3:26])[C:23](O)=[O:24]>>[CH3:1][C:2]1[CH:7]=[C:6]([N+:8]([O-:10])=[O:9])[CH:5]=[CH:4][C:3]=1[N:11]=[C:12]1[N:18]([CH2:17][CH:16]([CH2:19][CH3:20])[CH2:14][CH3:15])[C:23](=[O:24])[CH:22]([CH3:26])[S:13]1

Participants

4

Reactant 3

HCID 117342-Chloropropionic acidHCID 120492-Ethyl butylamineHCID 1456212-Methyl-4-nitrophenyl isothiocyanate

Product 1

HCID 18316267HCID 18316267, compound

Procedure

2-Methyl-4-nitrophenyl isothiocyanate was reacted with 2-ethyl-1-butylamine followed by α-chloropropionic acid according to Method C8a to afford 2-(2-methyl-4-nitrophenylimino)-3-(2-ethyl-1-butyl)-5-methyl-1,3-thiazolidin-4-one.

Sources & evidence

ORD record
ord-bbaba7aa49114553bafc341c695991fe
Source dataset
uspto-grants-2002_03
Patent number
US06353006B1

Reaction notes

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