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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2382208Generated: November 1, 2026

Ammonia → 4-Methoxy-alpha,alpha-dimethylcyclohexa-1,4-diene-1-methanol

https://huagongshe.com/reaction/2382208

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
Reactanttert-ButanolHCID 6386—
Reactant4-Methoxy-alpha,alpha-dimethylbenzyl alcoholHCID 81930—
ReactantLithiumHCID 3028194—
SolventTetrahydrofuranHCID 8028—
Product4-Methoxy-alpha,alpha-dimethylcyclohexa-1,4-diene-1-methanolHCID 645422674.2%

Reaction Conditions

Temperature-30 °C

Reaction Steps

2-(4-methoxy-phenyl)-propan-2-ol (750 g, 4.5 mol), anhydrous THF (7.5 L) and tert-BuOH (2001.4 g, 27 mol) were added under argon to a 22 L round bottomed flask equipped with an overhead stirrer, thermometer and dropping funnel. The mixture was cooled to −30° C. Gaseous ammonia was bubbled through the reaction mixture for 30 min. Granulated lithium (125 g, 18 mol) was added portion wise to the solution during 1-1.5 hr. The stirring was continued with slow flow of ammonia for 20 rh. The reaction was quenched with a solution of 961 g NH4Cl in 2.7 L water at −20° C. The top layer was separated and evaporated on a rotary evaporator at a bath temperature of 30° C. (all these and subsequent operations are performed under inert atmosphere). The aqueous layer was extracted with MTBE (3×1 L). The concentrate and extract were combined, washed with water and brine, dried over Na2SO4 and evaporated to dryness at a bath temperature of 35° C. The crude oily product was mixed with 725 ml Hexane and filtered. The filtrate was placed in a freezer at −70° C. and left for 24 hr. The solid was decanted and rinsed with Hexane pre-cooled to −70° C. (2×100 mL) with decantation after each rinsing. After drying under vacuum at 20° C., 562 g of the target product was obtained (yield 74%), having an HPLC purity of 89%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08258322B2
Source datasetuspto-grants-2012_09
ORD IDord-3d51ae6bd15e4a7b96d86d4af1da51a3
Source noteuspto-grants-2012_09