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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 128584Generated: October 30, 2026

Acetyl chloride → 2-Methoxy-4-(1-acetyl-4-piperidyloxy)benzoic acid

https://huagongshe.com/reaction/128584

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetyl chlorideHCID 6367—
ReactantTriethylamineHCID 8471—
Reactant2-Methoxy-4-(4-piperidyloxy)benzoic acidHCID 18914167—
SolventTetrahydrofuranHCID 8028—
Product2-Methoxy-4-(1-acetyl-4-piperidyloxy)benzoic acidHCID 18914145—

Reaction Steps

2-Methoxy-4-(4-piperidyloxy)benzoic acid (0.6 g, 2.09 mmol) was stirred in THF (10 ml) and treated with triethylamine (0.29 ml, 0.21 g, 2.08 mmol), followed by acetyl chloride (0.18 ml, 0.2 g, 2.5 mmol) and an additional 0.35 ml of triethylamine. The mixture was stirred at ambient temperature for 18 hours, then concentrated in vacuo. The residue was partitioned between aqueous sodium bicarbonate and ethyl acetate. The ethyl acetate layer was extracted with sodium bicarbonate solution. The combined sodium bicarbonate layers were acidified with 1N HCl and extracted with ethyl acetate. The organic layers were combined, washed with brine, dried over sodium sulfate, filtered, and evaporated to dryness in vacuo to give 2-methoxy-4-(1-acetyl-4-piperidyloxy)benzoic acid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05464788
Source datasetuspto-grants-1995_11
ORD IDord-720351c3d82047af9d81978a72b27c58
Source noteuspto-grants-1995_11