HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl 3-(2,3-difluoro-4-hydroxyphenyl)propanoate → HCID 85472984, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl 3-(2,3-difluoro-4-hydroxyphenyl)propanoate | HCID 90404786 | — |
| Reactant | HCID 90418025 | HCID 90418025 | — |
| Reactant | HCID 90418608 | HCID 90418608 | — |
| Product | HCID 85472984 | HCID 85472984 | — |
Reaction Steps
The title compound was prepared according to the procedure described in Example 197 by coupling of [5-chloro-3-(4-ethylphenyl)thiophen-2-yl]methanol and ethyl 3-(4-hydroxy-2,3-difluorophenyl)propanoate followed by hydrolysis of ethyl 3-(4-((5-chloro-3-(4-chlorophenyl)thiophen-2-yl)methoxy)-2,6-difluorophenyl)propanoate to afford the desired product as an off-white solid. 1H-NMR (300 MHz, CD3OD) δ 7.34 (d, J=8.1 Hz, 2H), 7.24 (d, J=8.1 Hz, 2H), 7.01 (s, 1H), 6.85 (d, J=9.3 Hz, 2H), 5.11 (s, 2H), 2.87 (t, J=7.2 Hz, 2H), 2.59-2.73 (m, 4H), 1.27 (t, J=7.8 Hz, 3H). Mass spectrum (ESI, m/z): Calcd. for C22H19C1F2O3S, 435.1 (M−H). found 435.1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09067898B1 |
| Source dataset | uspto-grants-2015_06 |
| ORD ID | ord-ee4ea421f6194e99917d04b763160c22 |
| Source note | uspto-grants-2015_06 |