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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1901150Generated: October 31, 2026

Water → HCID 21832206, compound

https://huagongshe.com/reaction/1901150

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant2-Amino-1-(3-chlorophenyl)ethan-1-olHCID 3751601—
Reactant5-[4-(2-Oxopropoxy)benzyl]thiazolidine-2,4-dioneHCID 21832150—
SolventBenzeneHCID 241—
ProductHCID 21832206HCID 2183220613.3%

Reaction Steps

A solution of 2.5 g of 2-amino-1-(3-chlorophenyl)ethanol (prepared as described in Preparation 8) and 3.58 g of 5-[4-(2-oxopropoxy)benzyl]thiazolidine -2,4-dione in 50 ml of benzene was heated under reflux for 1.5 hours, whilst the water being formed during the reaction was continuously removed. At the end of this time, the benzene used was removed by distillation under reduced pressure. The resulting residue was dissolved in 100 ml of absolute methanol, and then 3 g of sodium borohydride were added to the resulting solution. The reaction mixture was allowed to stand overnight at room temperature, after which it was concentrated by evaporation under reduced pressure, and the concentrate was mixed with water. The resulting aqueous mixture was extracted with ethyl acetate, and the extract was dried over anhydrous sodium sulfate. The solvent was removed by distillation under reduced pressure, and the resulting residue was purified by column chromatography through silica gel, using ethyl acetate, followed by a 10:1 by volume mixture of ethyl acetate and ethanol, as the eluent. The product was recrystallized from ethyl acetate, to give 0.74 g of the title compound as crystals, melting at 100°-125° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05576340
Source datasetuspto-grants-1996_11
ORD IDord-32941cdd5c6c45caadc676eae8b8b188
Source noteuspto-grants-1996_11