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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1357393Generated: November 2, 2026

Triethylamine → HCID 18506134, compound

https://huagongshe.com/reaction/1357393

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantBenzoyl chloride, 3-nitro-HCID 8495—
ReactantHCID 18506202HCID 18506202—
SolventAcetoneHCID 180—
SolventHCID 23286243HCID 23286243—
ProductHCID 18506134HCID 1850613481%

Reaction Steps

A mixture of 4-(2-aminophenoxy)phthalonitrile (0.5 g, 2.1 mmol), 3-nitrobenzoylchloride (0.43 g, 2.3 mmol) and triethylamine (0.54 g, 0.74 ml, 5.3 mmol) in acetone (20 ml) was stirred for 2 hours at room temperature. The mixture was evaporated in vacuo. The crude product was dissolved in methylene chloride (25 ml) and water (25 ml) and 1N hydrochloric acid (1 ml) was added. The water phase was extracted with methylene chloride (2×15 ml). The combined organic phase was dried over magnesium sulphate, filtered and evaporated in vacuo giving 700 mg of the crude product. The product was recystallised in acetone/pentane to give white crystals of N-[2-(3,4-dicyanophenoxy)phenyl]-3-nitrobenzamide (yield: 650 mg (81%)). Mp: 176.5-178.1° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06590118B1
Source datasetuspto-grants-2003_07
ORD IDord-527fd9e7596b4034844c5a8672a529f6
Source noteuspto-grants-2003_07