HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1160328Generated: October 26, 2026
Cesium carbonate → (+/-)-3-[4-(4-Trifluoromethyl-biphenyl-3-ylmethoxy)-phenyl]-3-(3-methylthiophen-2-yl)-propionic acid
https://huagongshe.com/reaction/1160328
Participants
| Role | Name | HCID | Charge |
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| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | 3-(4-Trifluoromethylphenyl)-benzyl chloride | HCID 22280138 | — |
| Reactant | (+/-)-Methyl 3-(4-hydroxyphenyl)-3-(3-methylthiophen-2-yl)propanoate | HCID 59132701 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | (+/-)-3-[4-(4-Trifluoromethyl-biphenyl-3-ylmethoxy)-phenyl]-3-(3-methylthiophen-2-yl)-propionic acid | HCID 86613226 | 85.9% |
Reaction Steps
Benzyl chloride 2.3 (113 mg, 0.434 mmol) and phenol 54.1 (100 mg, 0.362 mmol) were dissolved in acetone (1 mL) and treated with Cs2CO3 (371 mg, 1.14 mmol). The reaction was stirred at 50° C. for 16 h, filtered and concentrated. The residue was purified by column chromatography (silica gel, 30% to 60% ethyl acetate in hexanes). Eluant containing desired compound was concentrated and dissolved in a THF/MeOH/2N LiOH(aq) (1:1:1) solution (2 mL). The mixture was stirred at room temperature for 90 min., the solution was poured into 0.65 N HCl (aq.) (2 mL). The aqueous phase was extracted with dichloromethane (3×10 mL) and the combined organic phases were dried over Na2SO4. After filtration and drying, 154 mg (0.311 mmol) of carboxylic acid 54 was obtained. 1H NMR (400 MHz) (CDCl3) δ 7.43-7.70 (m, 8H), 7.21 (d, 2H, J=8.6 Hz), 7.05 (d, 1H, J=5.0 Hz), 6.92 (d, 2H, J=8.6 Hz), 6.76 (d, 1H, 5.0 Hz), 5.09 (s, 2H), 4.74 (t, 1H, J=7.8 Hz), 3.05 (d, 2H, J=7.8 Hz), 2.15 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07816367B2 |
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| Source dataset | uspto-grants-2010_10 |
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| ORD ID | ord-d40ad184df5940e1a43a37bfe88cfc4a |
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| Source note | uspto-grants-2010_10 |
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