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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | 4-Decylaniline | HCID 92309 | — |
| Reactant | Methyl 2-hydroxy-3-phenylbenzoate | HCID 241577 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-(4-decylphenyl)-2-hydroxy-[1,1'-biphenyl]-3-carboxamide | HCID 23043616 | 90% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04939133 |
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| Source dataset | uspto-grants-1990_07 |
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| ORD ID | ord-1edfb796a5e84ba8bb90232aa25fb128 |
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| Source note | uspto-grants-1990_07 |
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