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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 276293Generated: October 26, 2026

Triethylamine → 2-(2-Methyl-4-nitrophenylimino)-3-propanoyl-1,3-thiazolidine

https://huagongshe.com/reaction/276293

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantPropionyl chlorideHCID 62324—
ReactantHCID 178428748HCID 178428748—
SolventDichloromethaneHCID 6344—
Product2-(2-Methyl-4-nitrophenylimino)-3-propanoyl-1,3-thiazolidineHCID 1831605635%

Reaction Steps

To a solution of 2-(2-methyl-4-nitrophenylimino)-1,3-thiazolidine (prepared in a manner analogous to that described in Method C1a; 0.084 g, 0.35 mmol) in CH2Cl2 (5 mL) was added propionyl chloride (0.033 g, 0.35 mmol) and Et3N (0.049 mL, 0.35 mmol). The mixture was allowed to stir at room temp for 1 h, then was diluted with CH2Cl2 (40 mL). The resulting solution was sequentially washed with H2O (10 mL) and a saturated NaCl solution (10 mL), dried (Na2SO4), and concentrated under reduced pressure. The residue was purified by preparative TLC (40% EtOAc/hex) to give 2-(2-methyl-4-nitrophenylimino)-3-propanoyl-1,3-thiazolidine (0.036 g, 35%): FAB-MS m/z 294 ((M+H)+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06353006B1
Source datasetuspto-grants-2002_03
ORD IDord-30ad3212d8ac49f9b4ed2ab816253146
Source noteuspto-grants-2002_03