HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thionyl Chloride → 4-(1-Methylpiperidin-4-ylmethyl)-3-trifluoromethylbenzoyl chloride hydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | HCID 23145982 | HCID 23145982 | — |
| Product | 4-(1-Methylpiperidin-4-ylmethyl)-3-trifluoromethylbenzoyl chloride hydrochloride | HCID 23145933 | — |
Reaction Steps
This compound was prepared in the same manner as in Reference Example 1 (step 7), except that 4-(1-methylpiperidin-4-ylmethyl)-3-trifluoromethylbenzoic acid obtained in the step 2 was used, and that treatment after the reaction was that thionyl chloride was distilled off under reduced pressure, and then the operation of adding of toluene to the residue, followed by azeotropic removal of thionyl chloride was repeated twice.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07728131B2 |
| Source dataset | uspto-grants-2010_06 |
| ORD ID | ord-56c948ab8d044aadacf809da756b0e55 |
| Source note | uspto-grants-2010_06 |