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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 21440Generated: October 26, 2026

Pyridine → HCID 19931746, compound

https://huagongshe.com/reaction/21440

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant4-Vinylbenzoyl chlorideHCID 11052028—
Reactant1,2,3-Benzotriazin-4(1H)-oneHCID 135408793—
ProductHCID 19931746HCID 19931746—

Reaction Steps

A solution of benzo-1,2,3-triazin-4-one (3.8835 g) in dry pyridine (40 mL) was stirred, and to this solution was added, over a period of 30 seconds, freshly prepared 4-vinylbenzoyl chloride (4.3945 g, prepared as described in Hirao et al., Macromolecules, 21, 561 (1988)). The resultant reaction mixture was stirred at room temperature for 1.5 hours, then poured into an ice/water mixture (300 mL). The colorless precipitate which formed was filtered off, washed with water on the frit and dried. The dried product was then dissolved in methylene chloride (75 mL) and the resultant solution was washed with water, dried over anhydrous magnesium sulfate and passed through a short column of silica gel. The solution was then concentrated on a rotary evaporator to give the desired 3-(vinylbenzoyl)benzotriazinone product as a colorless solid (6.12 g) having melting point 120° C. The identity of the product was confirmed by proton nuclear magnetic resonance (NMR) and infra-red spectroscopy, the spectra being as follows:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05424268
Source datasetuspto-grants-1995_06
ORD IDord-64342a59a4714cb6b8cd229ac0523392
Source noteuspto-grants-1995_06