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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1179482Generated: October 30, 2026

N,N-Dimethylaniline → (2e)-3-{2,6-Difluoro-4-[(isopropoxycarbonyl)amino]phenyl}prop-2-enyl diazoacetate

https://huagongshe.com/reaction/1179482

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,N-DimethylanilineHCID 949—
ReactantTriethylamineHCID 8471—
ReactantGlyoxylyl Chloride p-toluenesulfonylhydrazoneHCID 57296158—
Reactantisopropyl 3,5-difluoro-4-[(1E)-3-hydroxyprop-1-enyl]phenylcarbamateHCID 58978084—
SolventDichloromethaneHCID 6344—
Product(2e)-3-{2,6-Difluoro-4-[(isopropoxycarbonyl)amino]phenyl}prop-2-enyl diazoacetateHCID 131726632—

Reaction Conditions

Temperature0 °C

Reaction Steps

Glyoxylic acid chloride p-toluenesulfonylhydrazone (4.64 g, 17.8 mmol) was added to a suspension of isopropyl 3,5-difluoro-4-[(1E)-3-hydroxyprop-1-enyl]phenylcarbamate (2.68 g, 9.89 mmol) in dichloromethane (66 mL). The mixture was cooled to 0° C. and treated with N,N-dimethylaniline (2.26 mL, 17.8 mmol). After 30 minutes, triethylamine (6.89 mL, 49.5 mmol) was added and the mixture stirred 30 minutes at 0° C. and 15 minutes at room temperature. The reaction mixture was then concentrated to ca. 15 mL and 50 mL of water added. The mixture was extracted with two portions of diethyl ether and the combined organic solutions washed with saturated NaHCO3, brine, and dried (MgSO4), filtered and concentrated. Purification by column chromatography (0-25% ethyl acetate-hexane) provided the title compound a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07279494B2
Source datasetuspto-grants-2007_10
ORD IDord-17a464035f7b48108458ace76583064d
Source noteuspto-grants-2007_10