Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1836527Generated: November 4, 2026

n-(4-Fluoro-2-trifluoromethyl-benzyl)-o-methyl-hydroxylamine → 2-(2,2-Dimethyl-5-oxo-[1,3]-dioxolan-4-ylidene)-n-(4-fluoro-2-trifluoromethyl-benzyl)-n-methoxy-acetamide

https://huagongshe.com/reaction/1836527

Reaction equation

Participants

RoleNameHCIDCharge
Reactantn-(4-Fluoro-2-trifluoromethyl-benzyl)-o-methyl-hydroxylamineHCID 23499553—
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-(4-fluoro-2-trifluoromethyl-benzyl)-n-methoxy-acetamideHCID 7385557598%

Reaction Steps

Reaction of (2,2-dimethyl-5-oxo-[1,3]dioxolan-4-ylidene)-acetyl chloride with N-(4-fluoro-2-trifluoromethyl-benzyl)-O-methyl-hydroxylamine as described in the preparation of compound 1-A gave the title amide as white crystals (98% yield): mp 129-130° C. (ethyl acetate-hexane). 1HNMR 400 MHz (CDCl3) δ (ppm): 1.76 (6H, s, CH3), 3.69 (3H, s, OCH3), 5.04 (2H, s, NCH2), 6.45 (1H, s, CH), 7.21 (1H, m, aromatic), 7.37 (1H, m, aromatic), 7.47 (1H, m, aromatic). Anal. calcd for C16H15F4NO5: C, 50.94; H, 4.01; N, 3.71. Found: C ,50.96; H, 4.07; N, 3.66.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06777440B2
Source datasetuspto-grants-2004_08
ORD IDord-3b5942e238cb441da7698de024fe83d0
Source noteuspto-grants-2004_08