HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1793003Generated: November 4, 2026
2-Fluoro-4-methylaniline → HCID 22025613, compound
https://huagongshe.com/reaction/1793003
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Fluoro-4-methylaniline | HCID 67984 | — |
| Reactant | 2,3,4-Trifluorobenzoic acid | HCID 302932 | — |
| Reactant | Lithium Hexamethyldisilazide | HCID 2733832 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 22025613 | HCID 22025613 | — |
Reaction Steps
2,3,4-Trifluorobenzoic acid and 2-fluoro-4-methylaniline were reacted in the presence of LiHMDS solution in THF by the general procedure of Example 1, Step B. After workup, 3,4-difluoro-2-[2-fluoro-4-methylanilino]benzoic acid was isolated as a crude pale brown solid which was reacted directly with 2-(aminooxy)ethanol and DMT-MM by the general procedure of Example 6, Step B below, then purified by column chromatography on silica gel (100% EtOAc as eluant) to give 3,4-difluoro-2-(2-fluoro-4-methylanilino)-N-(2-hydroxyethoxy)benzamide as a white solid (44%); m.p. (EtOAc/hexane) 134–139° C. 1H NMR [400 MHz, (CD3)2SO] [ ] 11.82 (v br s, 1H), 8.77 (br s, 1 H), 7.41 (ddd, J=8.1, 5.7, 1.6 Hz, 1 H), 7.13–7.00 (m, 2 H), 6.88 (dd, J=8.3, 1.1 Hz, 1 H), 6.82 (ddd, J=8.5, 8.5, 4.2 Hz, 1 H), 4.76 (v br s, 1 H), 3.86 (t, J=5.0 Hz, 2 H), 3.58 (J=5.0 Hz, 2 H), 2.25 (s, 3 H). Anal. calcd. for C16H15F3N2O3: C, 56.5; H, 4.4; N, 8.2. Found C, 56.3; H, 4.5; N, 8.2.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07078438B2 |
|---|
| Source dataset | uspto-grants-2006_07 |
|---|
| ORD ID | ord-652bcc1582d54f0ca58d7b36a9a67c78 |
|---|
| Source note | uspto-grants-2006_07 |
|---|