Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2197681Generated: October 23, 2026

5-(2-Chlorophenyl)furfural → HCID 86644300, compound

https://huagongshe.com/en/reaction/2197681

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-(2-Chlorophenyl)furfuralHCID 609821—
ReactantHCID 4594337HCID 4594337—
ReactantEthylenediamine diacetateHCID 10154317—
ReactantSodium BisulfiteHCID 23665763—
SolventMethanolHCID 887—
ProductHCID 86644300HCID 8664430092%

Reaction Steps

A mixture of 2-(4-oxo-2-thioxo-thiazolidin-3-ylamino)-benzoic acid (0.090 g, 0.34 mmol), 5-(2-chloro-phenyl)-furan-2-carbaldehyde (0.074 g, 0.36 mmol) (purchased from Aldrich Chemical Co.) and ethylenediamine diacetate (0.065 g, 0.036 mmol) in methanol (8 mL) was stirred at room temperature for 17 h. The reaction mixture was poured into stirred 0.6 N aq sodium hydrogensulfite (50 mL). The mixture was vigorously stirred for 15 min. The solid product was filtered off and washed on funnel successively with 0.6 N aq sodium hydrogensulfite (2 mL), water (2×2 mL), ether (2 mL) and hexanes (2 mL). The material was dried in a vacuum oven at 65° C. for 19 h to afford 2-{5-[1-[5-(2-Chloro-phenyl)-furan-2-yl]-methylidene]-4-oxo-2-thioxo-thiazolidin-3-ylamino}-benzoic acid (141 mg, 92%) as a solid. 1H NMR (400 MHz, DMSO-d6): δ 6.55 (1H, d, J=8.0 Hz), 6.87 (1H, t, J=7.6 Hz), 7.32 (1H, t, J=7.6 Hz), 7.44-7.51 (3H, m), 7.62 (1H, d, J=8.0 Hz), 7.66 (1H, d, J=8.4 Hz), 7.80 (1H, s), 7.91 (1H, d, J=8.0 Hz), 7.97 (1H, d, J=8.0 Hz). LC/MS: APCI 457.2, HPLC 97.9%

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08338465B2
Source datasetuspto-grants-2012_12
ORD IDord-8f1d28d31b87457bb8846e1a576c1406
Source noteuspto-grants-2012_12