HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl 2-(3,5-difluoro-4-hydroxyphenyl)cyclopropanecarboxylate → HCID 90418329, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl 2-(3,5-difluoro-4-hydroxyphenyl)cyclopropanecarboxylate | HCID 59419842 | — |
| Reactant | HCID 90418592 | HCID 90418592 | — |
| Product | HCID 90418329 | HCID 90418329 | — |
Reaction Steps
The title compound was prepared according to the procedure described in Example 1 following Steps 5 and 6 by coupling [3-(4-ethylphenyl)-5-(trifluoromethyl)-1,2-thiazol-4-yl]methyl methanesulfonate and ethyl 2-(3,5-difluoro-4-hydroxyphenyl)cyclopropane-1-carboxylate followed by hydrolysis to afford the desired product as an off-white solid. 1HNMR (300 MHz, CDCl3) δ 7.75 (d, J=8.1 Hz, 2H), 7.32 (d, J=8.1 Hz, 2H), 6.63-6.71 (m, 2H), 5.16 (s, 2H), 2.69-2.77 (m, 2H), 2.49-2.55 (m, 2H), 1.64-1.89 (m, 2H), 1.29-1.37 (m, 4H). Mass spectrum (ESI, m/z): Calcd. for C23H18F5NO3S, 482.1[M−H]. found 482.1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09067898B1 |
| Source dataset | uspto-grants-2015_06 |
| ORD ID | ord-fbc07d260d224a949ad3f217f4c2e5fc |
| Source note | uspto-grants-2015_06 |