HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 709459Generated: October 29, 2026
2-(5-Methyl-2-phenyl-4-oxazolyl)ethanol → HCID 66865094, compound
https://huagongshe.com/reaction/709459
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-(5-Methyl-2-phenyl-4-oxazolyl)ethanol | HCID 725585 | — |
| Reactant | 4-[2-[2-(4-Fluoro-phenyl)-ethylsulfanyl]-2-(2,2,2-trichloro-ethoxycarbonyl)-ethyl]-benzoic acid | HCID 66864823 | — |
| Reactant | HCID 86650303 | HCID 86650303 | — |
| Product | HCID 66865094 | HCID 66865094 | 91.5% |
Reaction Steps
The title compound was prepared from 4-[2-[2-(4-fluoro-phenyl)-ethylsulfanyl]-2-(2,2,2-trichloro-ethoxycarbonyl)-ethyl]-benzoic acid (220 mg, 0.46 mmol) and 2-(5-methyl-2-phenyl-oxazol-4-yl)-ethanol (103 mg, 0.50 mmol) in the same manner as described for 4-[2-[2-(4-fluoro-phenyl)-ethylsulfanyl]-2-(2,2,2-trichloro-ethoxy-carbonyl)-ethyl]-benzoic acid 2-phenyl-5-trifluoromethyl-oxazol-4-ylmethylester. The crude product was purified by flash chromatography using n-heptane/EtOAc 7:3 as the eluent to afford the final product as an oil (280 mg, 83.5%). 1H NMR (400 MHz, CDCl3): δ 7.91-7.96 (m, 3H), 7.39-7.41 (m, 3H), 7.22-7.25 (m, 3H), 7.06-7.09 (m, 2H), 6.94 (t, 2H), 4.71 (m, 1H), 4.64 (m, 1H), 4.56 (t, 1H), 3.88-3.92 (m, 2H), 3.55 (m 1H), 3.29 (m, 1H), 2.69-2.04 (m, 6H), 2.32 (s, 3H). Mass Spectrum: M+H+ 666.14, M−H+ 664.39.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09181181B2 |
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| Source dataset | uspto-grants-2015_11 |
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| ORD ID | ord-89a91d1ec2ec46d788c91e11b113b4d9 |
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| Source note | uspto-grants-2015_11 |
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