HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl 3-(2,3-difluoro-4-hydroxyphenyl)propanoate → HCID 85471823, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl 3-(2,3-difluoro-4-hydroxyphenyl)propanoate | HCID 90404786 | — |
| Reactant | HCID 90418562 | HCID 90418562 | — |
| Reactant | HCID 90418719 | HCID 90418719 | — |
| Product | HCID 85471823 | HCID 85471823 | — |
Reaction Steps
The title compound was prepared according to the procedure described in Example 208 by coupling of (2-(4-ethylphenyl)thiophen-3-yl)methanol and ethyl 3-(4-hydroxy-2,3-difluoro phenyl)propanoate followed by hydrolysis of ethyl 3-(4-((2-(4-ethylphenyl)thiophen-3-yl)methoxy)-2,3-difluorophenyl)propanoate to afford the desired product as an off-white solid. 1H NMR (400 MHz, CDCl3) δ 7.40 (d, J=7.1 Hz, 2H), 7.25 (m, 4H), 6.82 (t, J=6.5 Hz, 1H), 6.66 (t, J=6.5 Hz, 1H), 5.10 (s, 2H), 2.95 (t, J=7.5 Hz, 2H), 2.65 (t, J=7.0 Hz, 2H), 1.31 (t, J=9.5 Hz, 3H). LCMS (ESI, M/Z) for C22H20F2O3S: 403.1 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09067898B1 |
| Source dataset | uspto-grants-2015_06 |
| ORD ID | ord-be8251378e5043c4aa562d79ce3df4c8 |
| Source note | uspto-grants-2015_06 |