HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2121195Generated: November 2, 2026
3-Hydroxypyridine → 4-(3-Pyridyloxymethyl)2-phenylbenzoic acid methyl ester
https://huagongshe.com/reaction/2121195
Participants
| Role | Name | HCID | Charge |
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| Reactant | 3-Hydroxypyridine | HCID 7971 | — |
| Reactant | 18-Crown-6 | HCID 28557 | — |
| Reactant | Potassium bis(trimethylsilyl)amide | HCID 3251421 | — |
| Reactant | Methyl 4-bromomethyl-2-phenylbenzoate | HCID 18474540 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Product | 4-(3-Pyridyloxymethyl)2-phenylbenzoic acid methyl ester | HCID 10687098 | 48.4% |
Reaction Steps
To a mechanically-stirred 0° C. solution of 3-hydroxypyridine (4.4 g, 46 mmol) in DME (20 mL) was added potassium hexamethyldisilazide (0.5 M in toluene, 88.5 mL, 44 mmol) and the mixture was stirred for 15 minutes. 18-Crown-6 (1.46 g, 5.5 mmol) and a solution of 4-bromomethyl-2-phenylbenzoic acid methyl ester (6.8 g, 22 mmol) in toluene (25 mL) was added and the reaction mixture was vigorously stirred overnight. The reaction mixture was poured into 200 mL of water and the layers were separated. The aqueous phase was extracted with 2 portions of ethyl acetate and the combined organic phases were extracted with water and brine, dried (MgSO4), filtered and concentrated. The resulting oil was purified by flash chromatography (65% ethyl acetate-hexane) to give 4-(3-pyridyloxymethyl)-2-phenylbenzoic acid methyl ester (3.4 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06693123B2 |
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| Source dataset | uspto-grants-2004_02 |
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| ORD ID | ord-46f1714deabd407f83f5d6ccbca48c2c |
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| Source note | uspto-grants-2004_02 |
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