HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanesulfonyl chloride → HCID 13135954, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | n-Butyl 4-(piperazin-1-yl)-benzoate hydrochloride | HCID 20232632 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 13135954 | HCID 13135954 | — |
Reaction Steps
To a mixture of 27 g. (0.1 mole) n-butyl 4-(piperazin-1-yl)-benzoate hydrochloride and 270 ml. anhydrous pyridine are added at 5°-10° C. 11.4 g. (0.1 mole) methanesulphonyl chloride. The reaction mixture is left to stand overnight at 20° C. and then poured into 250 ml. ice water and extracted twice with methylene chloride. The extracts are dried with anhydrous sodium sulphate and evaporated in a vacuum. After trituration of the residue with ligroin, 17.1 g. (55% of theory) of the desired product are obtained as yellow crystals; m.p. 145°-150° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04616086 |
| Source dataset | uspto-grants-1986_10 |
| ORD ID | ord-03a46779aabb47b6ac699b7d67a9bb8b |
| Source note | uspto-grants-1986_10 |