1-Bromo-2-methylpropane → 2-(2-Methyl-4-nitrophenylimino)-3-isobutyl-1,3-thiazolidine

HRID 276313

Reaction equation

HRID 276313 reaction equation
[Cl-].Cl[CH2:3][CH2:4][NH3+:5].[CH3:6][C:7]1[CH:12]=[C:11]([N+:13]([O-:15])=[O:14])[CH:10]=[CH:9][C:8]=1[N:16]=[C:17]=[S:18].[CH2:19](Br)[CH:20]([CH3:22])[CH3:21]>>[CH3:6][C:7]1[CH:12]=[C:11]([N+:13]([O-:15])=[O:14])[CH:10]=[CH:9][C:8]=1[N:16]=[C:17]1[N:5]([CH2:19][CH:20]([CH3:22])[CH3:21])[CH2:4][CH2:3][S:18]1

Participants

4

Reactant 3

HCID 65551-Bromo-2-methylpropaneHCID 133682-Chloroethylammonium chlorideHCID 1456212-Methyl-4-nitrophenyl isothiocyanate

Product 1

HCID 183160642-(2-Methyl-4-nitrophenylimino)-3-isobutyl-1,3-thiazolidine

Procedure

2-Chloroethylammonium chloride (Entry 1) was reacted with 2-methyl-4-nitrophenyl isothiocyanate, which was reacted with isobutyl bromide according to Method D2a to give 2-(2-methyl-4-nitrophenylimino)-3-isobutyl-1,3-thiazolidine.

Sources & evidence

ORD record
ord-7bd3e815d99c47a49645b66ede2713fd
Source dataset
uspto-grants-2002_03
Patent number
US06353006B1

Linked notes

Loading…