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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1110284Generated: November 3, 2026

Trifluoroacetic acid → 3-(Octadecyloxy)-5-(phenylmethoxy)benzenamine

https://huagongshe.com/reaction/1110284

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
Reactant3-(Octadecyloxy)-5-(phenylmethoxy)phenylcarbamic acid dimethylethyl esterHCID 19389030—
SolventDichloromethaneHCID 6344—
Product3-(Octadecyloxy)-5-(phenylmethoxy)benzenamineHCID 1938895189%

Reaction Steps

A solution of 28 g of 3-(octadecyloxy)-5-(phenylmethoxy)phenylcarbamic acid dimethylethyl ester and 76 ml of trifluoroacetic acid in 700 ml of methylene chloride was kept at room temperature for 2 hours. The solution was concentrated at reduced pressure and the residue was extracted with methylene chloride. The extract was washed with NaHCO3 solution, dried and concentrated to a solid which was dissolved in 1000 ml of ether. The solution was treated with 21 ml of 3N HCl in ethanol. The hydrochloride salt which precipitated was filtered and treated with excess NaHCO3 to liberate the free base which was extracted with methylene chloride. The dried extract was concentrated at reduced pressure to give 20.4 g (89% yield, mp 57°-59°) of 3-(octadecyloxy)-5-(phenylmethoxy)benzenamine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05324747
Source datasetuspto-grants-1994_06
ORD IDord-1201da6a907b44afb7aa864a82f20c31
Source noteuspto-grants-1994_06