Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 26267Generated: October 25, 2026

Acetic Acid → trans-4-[2-(Dimethylamino)-ethyl]-4-cyclohexene-1,2-diol

https://huagongshe.com/reaction/26267

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantIodineHCID 807—
ReactantEthyl AcetateHCID 8857—
Reactant1-[2-(Dimethylamino)ethyl]-1,4-cyclohexadieneHCID 12228920—
CatalystSilver acetateHCID 11246—
Producttrans-4-[2-(Dimethylamino)-ethyl]-4-cyclohexene-1,2-diolHCID 54092690—

Reaction Steps

A solution of 45 g. (0.3 moles) of 1-[2-(dimethylamino)-ethyl]-1,4-cyclohexadiene from Example 3(a) in 1.5 l. of dry glacial acetic acid is treated with 100 g. of silver acetate and 75 g. of iodine. The mixture is stirred until most of the iodine dissolves and is then heated for two hours at 95°. The reaction solution is cooled, filtered and evaporated in vacuo to give an oil. The oil is taken up in ethyl acetate and washed with aqueous sodium bicarbonate solution. The organic phase is dried (MgSO4) and evaporated to an oil. The oil is taken up in ethyl acetate and treated with HCl in isoproanol. The resulting crude solid is removed by filtration and recrystallized from acetonitrile-ether to yield dl-trans-4-[2-(dimethylamino)-ethyl]-4-cyclohexene-1,2-diol, diacetate ester, hydrochloride salt.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04149001
Source datasetuspto-grants-1979_04
ORD IDord-2b7431e995a74a5fb28e43785fa3f5f3
Source noteuspto-grants-1979_04