HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2121165Generated: November 2, 2026
Methanol → 4-(3-Pyridyloxymethyl)2-phenylbenzoic acid
https://huagongshe.com/reaction/2121165
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methanol | HCID 887 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 4-(3-Pyridyloxymethyl)2-phenylbenzoic acid methyl ester | HCID 10687098 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-(3-Pyridyloxymethyl)2-phenylbenzoic acid | HCID 23436370 | 99.8% |
Reaction Steps
To 2.60 g (8.14 mmol) of 4-(3-pyridyloxymethyl)-2-phenylbenzoic acid methyl ester, prepared as in Example 187B, was added 15 mL of methanol, and a solution of 0.79 g (12 mmol) of 85% KOH in 3 mL of water. The mixture was stirred at reflux for 3 hours, then concentrated in vacuo. The residue was taken up in 5 mL of water and treated with 12 mL of 1M aqueous HCl. The precipitated product was filtered and washed with a small amount of water. The combined washings and filtrate were adjusted to pH 4 with 1M HCl, and additional precipitate was collected, then washed with water. The combined precipitates were dried in vacuo to give 4-(3-pyridyloxymethyl)-2-phenylbenzoic acid (2.48 g, 99%) as an off-white powder. 1H NMR (300 MHz, d6-DMSO) δ 5.31 (s, 2H), 7.31-7.56 (m, 9H), 7.76 (d, J=7.5 Hz, 1H), 8.19 (dd, J=1.0, 6.0 Hz, 1H), 8.39 (d, J=3.0 Hz, 1H), 12.8 (br s, 1H).
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-de2a9c61682542be9857379d9ad52906 |
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| Source note | uspto-grants-2004_02 |
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