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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2101713Generated: October 28, 2026

Formaldehyde → HCID 22066088, compound

https://huagongshe.com/reaction/2101713

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
ReactantFormamideHCID 713—
ReactantHCID 13602723HCID 13602723—
SolventWaterHCID 962—
ProductHCID 22066088HCID 22066088—

Reaction Conditions

Temperature205 °C

Reaction Steps

A mixture of (+/−)-2,2′,4,4′-tetrachlorobenzoin (1.0 gm, 2.9 mmol) from Step A and paraformaldehyde (0.70 gm, 24 mmol) in formamide (20 mL) was heated to 200-210° C. for 3 hr. The reaction was cooled to rt, diluted with water, and extracted twice with ethyl acetate. The organic layers were washed with brine, dried over sodium sulfate, and evaporated. The residue was purified by flash chromatography, eluting first with 10% ethyl acetate in hexanes to afford 4,5-di-(2,4-dichlorophenyl)oxazole as a higher Rf byproduct and then with 75% ethyl acetate in hexanes to elute the title compound as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07572785B2
Source datasetuspto-grants-2009_08
ORD IDord-c2091b4705df4570a003cce63cdf9a6b
Source noteuspto-grants-2009_08