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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2297514Generated: October 31, 2026

3-Phenoxybenzaldehyde → HCID 18381930, compound

https://huagongshe.com/reaction/2297514

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-PhenoxybenzaldehydeHCID 38284—
Reactant1-AcetylpiperazineHCID 83795—
ReactantSodium BicarbonateHCID 516892—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Solvent1,2-DichloroethaneHCID 11—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
ProductHCID 18381930HCID 1838193084.3%

Reaction Steps

3-phenoxybenzaldehyde (1.0 g) and 1-acetylpiperazine (739 mg) were dissolved in 1,2-dichloroethane (10 ml) and sodium triacetoxyboro hydride (1.72 g) and acetic acid (300 mg) were added. The atmosphere was replaced with argon and the mixture was stirred at room temperature for 6.5 hours. Water (5 ml) and saturated sodium hydrogen carbonate (20 ml) were added and the aqueous layer was extracted 5 times with chloroform. Organic layers were combined and dried over anhydrous sodium sulfate. Chloroform was removed and the residue was purified by silica gel column chromatography (ethyl adetate-ethyl acetate:methanol=20:1-10:1) to obtain 1.32 g of 1-acetyl-4-((3-phenoxyphenyl)methyl)piperazine. Yield: 84%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06492364B1
Source datasetuspto-grants-2002_12
ORD IDord-8571f5f648524339b9c8001bfb885b64
Source noteuspto-grants-2002_12