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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1413807Generated: November 2, 2026

Benzoyl chloride → HCID 20290849, compound

https://huagongshe.com/reaction/1413807

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl chlorideHCID 7412—
ReactantTriethylamineHCID 8471—
ReactantHCID 451690HCID 451690—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
ProductHCID 20290849HCID 2029084947.8%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 4,5-bis(4-methoxyphenyl)-2-nitroimidazole (3 g, 9.2 mmole) and triethylamine (3.9 ml., 27.6 mmole) in 30 ml. THF at 0° C. under N2 was dropwise added a solution of benzoyl chloride (1.2 ml., 10.1 mmole) in 5 ml THF. The reaction mixture was stirred for 8 hours at 0° C. and then left in the refrigerator overnight. The reaction was then diluted with 30 ml ether and filtered. The filtrate was concentrated on a rotary evaporator and chromatographed on Florisil. Recrystallization from methylcyclohexane gave 1.89 g of 1-benzoyl-4,5-bis(4-methoxyphenyl)-2-nitroimidazole, mp. 161°-163° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04251535
Source datasetuspto-grants-1981_02
ORD IDord-fda3a75af9cb49638d6d6d431a95afb6
Source noteuspto-grants-1981_02