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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2165096Generated: October 25, 2026

Tetrahydrofuran → N-(4-decylphenyl)-2-hydroxy-[1,1'-biphenyl]-3-carboxamide

https://huagongshe.com/reaction/2165096

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
Reactant4-DecylanilineHCID 92309—
ReactantMethyl 2-hydroxy-3-phenylbenzoateHCID 241577—
ReactantButyllithiumHCID 178418339—
SolventDichloromethaneHCID 6344—
ProductN-(4-decylphenyl)-2-hydroxy-[1,1'-biphenyl]-3-carboxamideHCID 2304361690%

Reaction Steps

To a tetrahydrofuran (20 ml) solution of 4-decylaniline (3.07 g, 13.14 mmol), cooled to 0°-5° C. (inert atmosphere), is added n-butyllithium (2.3 M, 13.14 mmol). The deeply colored solution is stirred for ten minutes, after which a tetrahydrofuran (20 ml) solution of methyl 3-phenylsalicylate (1.00 g, 4.38 mmol) is added. The temperature is allowed to rise to 25° C. over a 30 minute period. The reaction is quenched by pouring the contents into 10% hydrochloric acid (100 ml). The organics are extracted into ethyl acetate, washed with 10% hydrochloric acid, dried (sodium sulfate), and concentrated to give 2.77 g of crude solid. Chromatography (Kieselgel 60, dichloromethane) affords N-(4-decylphenyl)-2-hydroxy-[1,1'-biphenyl]-3-carboxamide (1.69 g, 90%), mp 74°-75° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04939133
Source datasetuspto-grants-1990_07
ORD IDord-1edfb796a5e84ba8bb90232aa25fb128
Source noteuspto-grants-1990_07