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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2181142Generated: November 2, 2026

n-[3-(4-Fluorophenyl)-propyl]-o-methyl-hydroxylamine → 2-(2,2-Dimethyl-5-oxo-[1,3]-dioxolan-4-ylidene)-n-[3-(4-fluorophenyl)-propyl]-n-methoxy-acetamide

https://huagongshe.com/reaction/2181142

Reaction equation

Participants

RoleNameHCIDCharge
Reactantn-[3-(4-Fluorophenyl)-propyl]-o-methyl-hydroxylamineHCID 22485663—
Reactant(2,2-Dimethyl-5-oxo-[1,3]dioxolan-4-ylidene)-acetyl chlorideHCID 85435482—
Product2-(2,2-Dimethyl-5-oxo-[1,3]-dioxolan-4-ylidene)-n-[3-(4-fluorophenyl)-propyl]-n-methoxy-acetamideHCID 7385558797%

Reaction Steps

Reaction of (2,2-dimethyl-5-oxo-[1,3]dioxolan-4-ylidene)-acetyl chloride with N-[3-(4-fluorophenyl)-propyl]-O-methyl-hydroxylamine as described in the preparation of compound 1-C gave the title amide as white crystals (97% yield): mp 90-91° C. (ethyl acetate-hexane). 1HNMR 400 MHz (CDCl3) δ (ppm): 1.77 (6H, s, CH3), 1.98 (2H, m, CH2), 2.64 (2H, t, J=7.9 Hz, CH2), 3.71 (2H, t, J=7.6 Hz, NCH2), 3.73 (3H, s, OCH3), 6.41 (1H, broad s, CH), 6.98 (2H, m, aromatics), 7.16 (2H, m, aromatics). Anal. calcd for C17H20FNO5: C, 60.53; H, 5.98; N, 4.15. Found: C, 60.43; H, 5.99; N, 4.09.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06890942B2
Source datasetuspto-grants-2005_05
ORD IDord-d525e34a5c024403a9e7be75361be4db
Source noteuspto-grants-2005_05