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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1396126Generated: November 2, 2026

Acetyl chloride → HCID 58387042, compound

https://huagongshe.com/reaction/1396126

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetyl chlorideHCID 6367—
ReactantTriethylamineHCID 8471—
ReactantHCID 58387097HCID 58387097—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 58387042HCID 58387042—

Reaction Steps

The compound ‘carbamic acid 3-[4-(4-hydroxy-phenyl)-piperazin-1-yl]-3-oxo-1-phenyl-propyl ester (2 mmol)’ prepared in Example 18 was dissolved in tetrahydrofuran 25 mL), and triethylamine (2.4 mmol) and acetylchloride (2.4 mmol) were added to the mixture. The reslting mixture was stirred at a room temperature for 5 hours. Then, the reaction mixture was diluted with water, and extracted several times with ethyl acetate to obtain an organic phase. The prepared organic phase was dried over magnesium sulfate, and concentrated under a reduced pressure. The resulting pellet was purified with column chromatography (hexane:ethyl acetate=1:1) to obtain a title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08901116B2
Source datasetuspto-grants-2014_12
ORD IDord-ed3c098db8864814930ee9d19a8fa854
Source noteuspto-grants-2014_12