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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2050210Generated: October 31, 2026

Methanol → 4-(1-Adamantyloxy)-N-methyl-N-[3-(dimethylamino)propyl]aniline

https://huagongshe.com/reaction/2050210

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantN-Methyl-p-(1-adamantyloxy)anilineHCID 12510299—
Reactant(1-Chloropropyl)dimethylamineHCID 22278018—
ReactantButyllithiumHCID 178418339—
SolventTolueneHCID 1140—
SolventPentaneHCID 8003—
SolventTetrahydrofuranHCID 8028—
Product4-(1-Adamantyloxy)-N-methyl-N-[3-(dimethylamino)propyl]anilineHCID 12510329—

Reaction Steps

To an ice:MeOH cooled solution of 2.0 g. (0.078 mole) of N-methyl-p-(1-adamantyloxy)aniline in 20 ml. THF was added 4.75 ml. of 1.64 N BuLi in pentane. A solution of a 1:1 mixture of toluene and 1-chloro-N,N-dimethyl propyl amine in 20 ml. THF was then added and the mixture stirred at room temperature for 1 hour and at reflux for 20 hours. The bulk of the solvent was removed in vacuum and the residue dissolved in H2O and Et2O. The organic layer was washed with H2O and brine and taken to dryness. The residue was dissolved in CH2Cl2, treated with an excess of HCl in Et2O and taken to dryness. The remaining solid was recrystallized from MeOH:CH3CN to give 1.72 g. (53%) of 4'-(1-adamantyloxy)-N-methyl-N-[3-(dimethylamino)propyl]aniline, m.p. 221°-223°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04200588
Source datasetuspto-grants-1980_04
ORD IDord-f52bc419c27943649cc63233a51eb0c4
Source noteuspto-grants-1980_04