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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 372344Generated: October 27, 2026

Boron trifluoride etherate → 2-(2,4-Dichlorophenoxymethyl)-4-thiazolidinone

https://huagongshe.com/reaction/372344

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoron trifluoride etherateHCID 8000—
Reactant2-MercaptoacetamideHCID 12961—
Reactant2,4-DichlorophenoxyacetaldehydeHCID 5092937—
SolventDiethyl EtherHCID 3283—
Product2-(2,4-Dichlorophenoxymethyl)-4-thiazolidinoneHCID 1239149420.1%

Reaction Steps

To a solution containing 5.25g (0.025 mole) of (2,4-dichlorophenoxy)acetaldehyde and 5.0g (0.055 mole) of thioglycolamide in 100 ml of anhydrous ether was added 14.2g (0.10 mole) of boron trifluoride etherate. The resulting solution was stirred at ambient temperature for 6 hours, washed with water, dried (MgSO4), and concentrated to dryness. The residual solid was purified by silica chromatography to give 1.4g of 2-(2,4-dichlorophenoxymethyl)-4-thiazolidinone as a white crystalline solid melting at 134°-136°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04090861
Source datasetuspto-grants-1978_05
ORD IDord-3f8a4448b3094ec4859c52174c3695e1
Source noteuspto-grants-1978_05