HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 86638743, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | Phenylmethyl 4-(1-hydroxyethyl)-1-piperidinecarboxylate | HCID 18918437 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 86638743 | HCID 86638743 | — |
Reaction Steps
A solution of methanesulphonyl chloride (0.85 ml) in dichloromethane (20 ml) was added dropwise to a stirred, ice-cooled solution of triethylamine (1.55 ml) and the product of step i) (2.64 g) in dichloromethane (50 ml). After stirring for 3 hours the reaction mixture was washed with water (3×) and brine, dried (PS paper) and evaporated in vacuo to yield N-benzyloxycarbonylpiperidin-4-ylethanol mesylate as a colourless paste (3.4 g) NMR (d6DMSO) δ 0.9-1.2(2H,m); 1.5-1.8(5H,m); 2.6-2.9(2H,m); 4.0(2H,d); 4.25(2H,t); 4.4(3H,s); 5.1(2H,s); 7.35(5H,m); m/e 342 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05750754 |
| Source dataset | uspto-grants-1998_05 |
| ORD ID | ord-e469c09be9db4cbf813507f451af1a07 |
| Source note | uspto-grants-1998_05 |