HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1610592Generated: October 31, 2026
Benzyl 4-Hydroxybenzoate → HCID 22261396, compound
https://huagongshe.com/reaction/1610592
Participants
| Role | Name | HCID | Charge |
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| Reactant | Benzyl 4-Hydroxybenzoate | HCID 7180 | — |
| Reactant | 2-Bromopyridine | HCID 7973 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Catalyst | Copper | HCID 23978 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 22261396 | HCID 22261396 | — |
Reaction Steps
To a solution of benzyl 4-hydroxybenzoate (25.3 g, 111 mmol) in N,N-dimethylformamide (60 ml) was added potassium tert-butoxide (12.4 g, 111 mmol), and the mixture was stirred at room temperature for 1 hr. The reaction solution was evaporated under reduced pressure and 2-bromopyridine (24.5 g, 155 mmol), a copper powder (1.76 g, 27.7 mmol) and N,N-imethylformamide (80 ml) were added. The mixture was stirred at 120° C. for 8 hrs. The reaction solution was filtered with celite, and the filtrate was evaporated under reduced pressure. To the residue was added water (500 ml), and the mixture was extracted with ethyl acetate (500 ml). The extract was washed successively with water and saturated brine, dried (anhydrous magnesium sulfate) and evaporated under reduced pressure. The residue was purified by silica gel column chromatography (hexane:ethyl acetate=10:1). Recrystallization from ethyl acetate-hexane gave the objective substance (25.5 g, 73%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06982348B2 |
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| Source dataset | uspto-grants-2006_01 |
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| ORD ID | ord-7b824920d969412eaad66c3e3c286d1b |
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| Source note | uspto-grants-2006_01 |
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