HuagongsheHuagongshe Chemistry Print Report · For research reference only
Chlorosulfonic acid → 4-Methoxy-3-[4-(2,2,2-trifluoro-acetyl)-piperazin-1-yl]-benzenesulfonyl chloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Chlorosulfonic acid | HCID 24638 | — |
| Reactant | 2,2,2-Trifluoro-1-[4-(2-methoxyphenyl)piperazin-1-yl]ethanone | HCID 3788144 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-Methoxy-3-[4-(2,2,2-trifluoro-acetyl)-piperazin-1-yl]-benzenesulfonyl chloride | HCID 12136655 | — |
Reaction Steps
A solution of 2,2,2-trifluoro-1-[4-(2-methoxy-phenyl)-piperazin-1-yl]-ethanone (14 g; 0.48 mol) in dichloromethane (20 mL) was added to chlorosulfonic acid (75 mL) in such a rate that the inner temperature did not exceed −5° C. After 10 min at this temperature, the solution was poured slowly onto ice-water (500 g), the precipitate was filtered and washed with cold water (2×200 mL) and cold diethyl ether (200 mL). The resulting solid was recrystallized from diethyl ether to give 4-methoxy-3-[4-(2,2,2-trifluoro-acetyl)-piperazin-1-yl]-benzenesulfonyl chloride as white powder (7.7 g; 41%), MS, MH+ 387, m. p. 125-127.3° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06825202B2 |
| Source dataset | uspto-grants-2004_11 |
| ORD ID | ord-c3aaa121bad34acfb7ffad3fdc4969cd |
| Source note | uspto-grants-2004_11 |