HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-(5-Methyl-2-phenyloxazol-4-yl)ethyl 4-methylbenzenesulfonate → HCID 22340068, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-(5-Methyl-2-phenyloxazol-4-yl)ethyl 4-methylbenzenesulfonate | HCID 12051739 | — |
| Reactant | HCID 69314709 | HCID 69314709 | — |
| Product | HCID 22340068 | HCID 22340068 | — |
Reaction Steps
Standard Procedure (B) was utilized to prepare the title compound from 3-(4-hydroxy-phenyl)-2-methyl-2-(3-trifluoromethyl-phenoxy)-propionic acid ethyl ester and toluene-4-sulfonic acid 2-(2-phenyl-5-methyl-oxazol-4-yl)-ethyl ester. 1H NMR (400 MHz, CDCl3) δ 7.99-7.97 (m, 2H), 7.50-7.46 (m, 3H), 7.33 (t, 1H, J=8.21 Hz), 7.26-7.24 (m, 1H), 7.17 (d, 2H, J=8.60 Hz), 7.14-7.12 (m, 1H), 7.04-7.01 (m, 1H), 6.81 (d, 2H, J=8.60 Hz), 4.20 (t, 2H, J=5.87 Hz), 3.27 (d, 1H, J=14.08 Hz), 3.14 (d, 1H, J=14.08 Hz), 3.07 (t, 2H, J=5.87 Hz), 2.42 (s, 3H), 1.44 (s, 3H); HRMS (ES+) m/z exact mass calcd for C29H27NO5F3 526.1841, found 526.1845.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06930120B2 |
| Source dataset | uspto-grants-2005_08 |
| ORD ID | ord-d645b3af21f64afab55e8ede4de22d3a |
| Source note | uspto-grants-2005_08 |