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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2402346Generated: October 31, 2026

HCID 45084195, compound → {3-[Bis(4-methoxybenzyl)amino]-4-chlorophenyl}(1-methylcyclopropyl)methanone

https://huagongshe.com/reaction/2402346

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 45084195HCID 45084195—
Reactant2-Chloro-5-iodo-N,N-bis(4-methoxybenzyl)anilineHCID 70873300—
ReactantHCID 178418918HCID 178418918—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
Product{3-[Bis(4-methoxybenzyl)amino]-4-chlorophenyl}(1-methylcyclopropyl)methanoneHCID 70873254—

Reaction Conditions

Temperature-78 °C

Reaction Steps

Under argon, 7.587 g (15.37 mmol) of 2-chloro-5-iodo-N,N-bis(4-methoxybenzyl)aniline were dissolved in 100 ml of THF and cooled to −78° C. 7.65 ml (15.27 mmol) of a 2 M solution of isopropylmagnesium chloride in diethyl ether were then slowly added dropwise. The reaction solution was then slowly warmed to −40° C. and stirred at this temperature for 30 min. 2 g (13.97 mmol) of N-methoxy-N,1-dimethylcyclopropanecarboxamide [R. Shintani et al., Chem. Eur. J., 15 (35), 8692-8694 (2009)], dissolved in 20 ml of THF, were then slowly added dropwise to the reaction solution. The reaction mixture obtained was then slowly warmed to room temperature and stirred at this temperature overnight. 50 ml of an ice-cold saturated aqueous ammonium chloride solution were then added to the reaction mixture. After separation of the phases, the aqueous phase was extracted three more times with ethyl acetate, and the combined organic phases were dried over magnesium sulphate, filtered and evaporated to dryness. The crude product obtained was purified chromatographically on silica gel (mobile phase cyclohexane/ethyl acetate 10:1). This gave 3.977 g (63% of theory) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08796335B2
Source datasetuspto-grants-2014_08
ORD IDord-89f1265449524566aad48ba487069e1c
Source noteuspto-grants-2014_08