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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1836524Generated: November 4, 2026

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

https://huagongshe.com/reaction/1836524

Reaction equation

Participants

RoleNameHCIDCharge
Reactanto-Methyl-n-(4-trifluoromethyl-benzyl)-hydroxylamineHCID 23499567—
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-methoxy-n-(4-trifluoromethylbenzyl)-acetamideHCID 7385554897%

Reaction Steps

Reaction of (2,2-dimethyl-5-oxo-[1,3]dioxolan-4-ylidene)-acetyl chloride with O-methyl-N-(4-trifluoromethyl-benzyl)-hydroxylamine as described in the preparation of compound 1-A gave the title amide as white crystals (97% yield): mp 110° C. (ethyl acetate-hexane). 1HNMR 400 MHz (CDCl3) δ (ppm): 1.76 (6H, s, CH3), 3.71 (3H, s, OCH3), 4.87 (2H, s, NCH2), 6.40 (1H, s, CH), 7.47 (2H, m, aromatics), 7.59 (2H, m, aromatics). Anal. calcd for C16H16F3NO5: C, 53.49; H, 4.49; N, 3.90. Found: C, 53.48; H, 4.53; N, 3.83.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06777440B2
Source datasetuspto-grants-2004_08
ORD IDord-73564fc522124135baff78df4458efe1
Source noteuspto-grants-2004_08