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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1017821Generated: October 26, 2026

Water → N-(4-((3-(4-Isopropylphenyl)-2-methyl-2-propenyl)oxy)-2,3,6-trimethylphenyl)formamide

https://huagongshe.com/reaction/1017821

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium hydrideHCID 24758—
ReactantN-(4-hydroxy-2,3,6-trimethylphenyl)formamideHCID 21961295—
Reactant1-(3-Bromo-2-methyl-1-propenyl)-4-isopropylbenzeneHCID 68707986—
SolventDimethylformamideHCID 6228—
ProductN-(4-((3-(4-Isopropylphenyl)-2-methyl-2-propenyl)oxy)-2,3,6-trimethylphenyl)formamideHCID 7385674663%

Reaction Steps

To a solution of N-(4-hydroxy-2,3,6-trimethylphenyl)formamide (3.00 g, 16.7 mmol) in N,N-dimethylformamide (30 ml) was added at 0° C. under a nitrogen atmosphere sodium hydride (a 60% dispersion in liquid paraffin, 0.74 g, 18.4 mmol) and the resulting mixture was stirred at the same temperature for 10 minutes. To the reaction solution was added 1-(3-bromo-2-methyl-1-propenyl)-4-isopropylbenzene (4.66 g, 18.4 mmol) and the resulting mixture was stirred at room temperature for 30 minutes. Water was added into the reaction solution and the product was extracted twice with ethyl acetate. The combined extracts were washed with water, dried on magnesium sulfate, and then concentrated under reduced pressure. The resulting residue was crystallized from ethyl acetate-hexane to obtain 3.70 g (63% yield) of the title compound. Melting point: 153-155° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06479536B1
Source datasetuspto-grants-2002_11
ORD IDord-c45122ecb0214f45994b27dede8aea3c
Source noteuspto-grants-2002_11