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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1612949Generated: October 29, 2026

Hydrochloric Acid → 2-Acetyl-5-[3-(cyclopentyloxy)-4-methoxyphenyl]-1-methyl-3-pyrazolidinone hydrochloride

https://huagongshe.com/reaction/1612949

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantAcetic AnhydrideHCID 7918—
Reactant5-[3-(Cyclopentyloxy)-4-methoxyphenyl]-1-methyl-3-pyrazolidinoneHCID 19792765—
SolventDiethyl EtherHCID 3283—
Product2-Acetyl-5-[3-(cyclopentyloxy)-4-methoxyphenyl]-1-methyl-3-pyrazolidinone hydrochlorideHCID 1979278998%

Reaction Steps

5-[3-(Cyclopentyloxy)-4-methoxyphenyl]-1-methyl-3-pyrazolidinone (0.500 g) is dissolved in acetic anhydride (15 mL). The resulting solution is warmed to reflux for 2 hours, cooled to room temperature and concentrated in vacuo to afford an oil. This residue is dissolved in ether and treated with ethanolic HCl at room temperature. The resulting solid is stirred for 4 hours at room temperature, collected by suction and dried in vacuo to afford the title compound as a white powder (0.621 g; 98%) mp: 82°-85° C. 1H NMR (DMSO-d6, 400 MHz) δ6.88 (m, 3H); 3.85 (s, 3H); 2.82 (s, 3H); 2.52 (s, 3H); 2.00 (m, 2H); 1.84 (m, 3H); 1.64 (m, 2H). IR (KBr, cm-1) 1730.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05191084
Source datasetuspto-grants-1993_03
ORD IDord-ab47c019473347648edb80b5d9b6419b
Source noteuspto-grants-1993_03