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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 566879Generated: November 1, 2026

Acetic Acid → HCID 9902382, compound

https://huagongshe.com/reaction/566879

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactant1-(p-Tolyl)piperazineHCID 83113—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantHCID 54197501HCID 54197501—
Solvent1,2-DichloroethaneHCID 11—
ProductHCID 9902382HCID 990238233%

Reaction Steps

A mixture of 3-oxo-dihydro-2H-benzo[1,4]oxazine-7-carbaldehyde (0.5 g, 2.8 mmol), 1-(4-methyl-phenyl)-piperazine (0.5 g, 2.8 mmol), acetic acid (0.17 g, 2.8 mmol) and sodium triacetoxyborohydride (1.2 g, 5.9 mmol) in 20 mL of 1,2-dichloroethane is stirred at room temperature for 3 hours. The reaction is quenched with 50 mL of water, and the layers are separated. The aqueous phase is extracted with ethyl acetate (3×50 mL). The organic phases are combined and dried over sodium sulfate. Evaporation of the solvent gives a solid which is recrystallized twice from acetonitrile to give 0.31 g (33% yield) of 7-[4-(4-methyl-phenyl)-piperazin-1-ylmethyl]-4H-benzo[1,4]oxazine-3-one; mp 208-210° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06177422B1
Source datasetuspto-grants-2001_01
ORD IDord-f959548f6c9e4548b1f9e07edb94748f
Source noteuspto-grants-2001_01