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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Butyl isocyanate | HCID 8110 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 3-Trifluoromethyl-4'-hydroxy-alpha-ethylbenzhydrol | HCID 181876 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | 1-(3-Trifluoromethylphenyl)-1-(4-butylaminocarbonyloxyphenyl)-1-propanol | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04564630 |
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| Source dataset | uspto-grants-1986_01 |
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| ORD ID | ord-f076cec6be3d4570b8a05b9fb53c40d8 |
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| Source note | uspto-grants-1986_01 |
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