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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1284927Generated: October 27, 2026

Butyl isocyanate → 1-(3-Trifluoromethylphenyl)-1-(4-butylaminocarbonyloxyphenyl)-1-propanol

https://huagongshe.com/reaction/1284927

Reaction equation

Participants

RoleNameHCIDCharge
ReactantButyl isocyanateHCID 8110—
ReactantTriethylamineHCID 8471—
ReactantPotassium HydroxideHCID 14797—
Reactant3-Trifluoromethyl-4'-hydroxy-alpha-ethylbenzhydrolHCID 181876—
SolventBenzeneHCID 241—
Product1-(3-Trifluoromethylphenyl)-1-(4-butylaminocarbonyloxyphenyl)-1-propanolHCID 14727324—

Reaction Steps

8.9 g. of 3-trifluoromethyl-4'-hydroxy-α-ethyl-benzhydrol, 3.3 g. of n-butyl-isocyanate and 0.06 ml. of triethyl amine in 45 ml. of dry benzene are heated up to 50° C. under stirring, and the reaction mixture is kept at the same temperature for one additional hour. The progress of the reaction is monitored by thin layer chromatography. When the reaction is complete, the mixture is cooled to room temperature, the benzene solution is shaken with a 5% aqueous potassium hydroxide solution and washed to neutral with water. The organic phase is dried over anhydrous magnesium sulfate, filtered, and the solvent is distilled off under reduced pressure. The solid residue is crystallized from a mixture of ethyl acetate and n-hexane. 11.4 g. of the named compound are obtained, melting at 99° to 100° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04564630
Source datasetuspto-grants-1986_01
ORD IDord-f076cec6be3d4570b8a05b9fb53c40d8
Source noteuspto-grants-1986_01