HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 21883557, compound → HCID 21883547, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 21883557 | HCID 21883557 | — |
| Reactant | Potassium hydroxy sulfite | HCID 23707502 | — |
| Product | HCID 21883547 | HCID 21883547 | — |
Reaction Steps
Following a procedure similar to that described in Example 128, ethyl 6-chloro-7-[(4-chlorophenyl)thio]-2-(trifluoromethyl)-2H-1-benzopyran-3-carboxylate (Example 192) was treated with OXONE® yielding the products labeled Example 193 and Example 194: mp 213.8–217.4° C. 1H NMR (acetone-d6/300 MHz) 7.91 (s, 1H), 7.83 (d, 2H, J=8.7 Hz), 7.62 (m, 4H), 5.98 (q, 1H, J=6.8 Hz). 19F NMR (acetone-d6/282 MHz) −79.3 (d, J=7.2 Hz). ESLRMS m/z 435 (M−H). ESHRMS m/z 434.9470 (M−H, Calc'd 434.9472). Anal. Calc'd for C17H9Cl2F3O4S: C, 46.70; H, 2.07; Cl, 16.22; S, 7.33. Found: C, 46.80; H, 2.28; Cl, 16.75; S, 7.39.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07138411B2 |
| Source dataset | uspto-grants-2006_11 |
| ORD ID | ord-5c7af4acda8a451ca59663dc735d1f33 |
| Source note | uspto-grants-2006_11 |