HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 226506Generated: October 28, 2026
1,2-Dimethoxyethane → Ethyl [5-benzyloxy-4'-(trifluoromethyl)biphenyl-3-yl]acetate
https://huagongshe.com/reaction/226506
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,2-Dimethoxyethane | HCID 8071 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 4-(Trifluoromethyl)phenylboronic acid | HCID 2734389 | — |
| Reactant | (3-Benzyloxy-5-trifluoromethanesulfonyloxy-phenyl)-acetic acid ethyl ester | HCID 57755048 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Ethyl [5-benzyloxy-4'-(trifluoromethyl)biphenyl-3-yl]acetate | HCID 24771790 | 100% |
Reaction Steps
A mixture of (3-benzyloxy-5-trifluoromethanesulfonyloxy-phenyl)-acetic acid ethyl ester (108 g, 0.26 mol), 4-(trifluoromethyl)phenylboronic acid (55.6 g, 0.29 mol), 1,2-dimethoxyethane (1.1 L) and aqueous Na2CO3 (2 M, 129 mL, 0.26 mol) was mechanically stirred while purging N2 at room temperature for 10 min. To this system was added Pd(Ph3)4 (480 mg, 0.42 mmol) and heated to reflux (95° C.) for 2.5 h. The red-brown mixture was diluted with EtOAc (0.5 L) and washed with saturated aqueous NaHCO3 solution (3×200 mL) and brine (2×200 mL). The organic fraction was dried (Na2SO4) and concentrated in vacuo. The crude mixture was purified by ISCO column chromatography to obtain (5-benzyloxy-4′-trifluoromethyl-biphenyl-3-yl)-acetic acid ethyl ester (107 g, 100%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07557244B2 |
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| Source dataset | uspto-grants-2009_07 |
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| ORD ID | ord-148992f9ba5b473fadef74067bc520a3 |
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| Source note | uspto-grants-2009_07 |
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