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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1830145Generated: October 27, 2026

2-(2-Morpholin-4-yl-2-oxoethyl)-5-phenyl-pentanoic acid ethyl ester → 2-(2-morpholin-4-yl-2-oxo-ethyl)-5-phenyl-pentanoic Acid

https://huagongshe.com/reaction/1830145

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(2-Morpholin-4-yl-2-oxoethyl)-5-phenyl-pentanoic acid ethyl esterHCID 21031026—
ReactantMethanol--water (1/1)HCID 22242641—
Product2-(2-morpholin-4-yl-2-oxo-ethyl)-5-phenyl-pentanoic AcidHCID 985767389%

Reaction Steps

To a solution of 2-(2-morpholin-4-yl-2-oxo-ethyl)-5-phenyl-pentanoic acid ethyl ester (604 mg, 1.81 mmol) in a 2:1 mixture of MeOH—H2O (12 ml) LiOH.H2O (228 mg, 5.43 mmol) was added and stirred overnight at room temperature. Ethanol was removed under reduced pressure, residue diluted with water (40 ml) and washed with ether. The aqueous layer was acidified to pH1 with 1N HCl and extracted with diethyl ether (3×25 ml). The combined organic extracts were dried with MgSO4 and concentrated under reduced pressure to give 2-(2-morpholin-4-yl-2-oxo-ethyl)-5-phenyl-pentanoic acid as a white solid (492 mg); 1H NMR (CDCl3) 8.0–7.5 (1H), 7.4–7.1 (m, 5H), 3.8–3.4 (m, 8H), 3.0 (m, 1H), 2.8 (dd, J=16.4, 9.6 Hz, 1H), 2.65 (t, J=7.2 Hz, 2H), 2.40 (dd, J=16.4, 4.3 Hz, 1H), 1.9–1.5 (m, 4H). MS: 306 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07064123B1
Source datasetuspto-grants-2006_06
ORD IDord-6af270b1e84f49d294e6459f03ce5d2a
Source noteuspto-grants-2006_06