HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 1-(4-Cyanophenyl)-4-mesyloxymethyl-piperidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | 4-(4-(Hydroxymethyl)piperidin-1-yl)benzonitrile | HCID 19391296 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-(4-Cyanophenyl)-4-mesyloxymethyl-piperidine | HCID 19391270 | — |
Reaction Steps
To a solution of 5.5 g of 1-(4-cyanophenyl)-4-hydroxymethyl-piperidine and 5.16 g of triethylamine in 150 ml of methylene chloride, 5.84 g of methanesulphonic acid chloride are slowly added dropwise at ambient temperature and with stirring. After it has all been added the mixture is left to stand overnight and the solvent is removed under reduced pressure. The residue is chromatographed with methylene chloride/methanol (50:1) over silica gel. Yield: 6.95 g (93% of theory), Mass spectrum: (M+H)+ =295
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05442064 |
| Source dataset | uspto-grants-1995_08 |
| ORD ID | ord-70d7912ec63f40edb04c7797831045c4 |
| Source note | uspto-grants-1995_08 |