HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl 1-(phenylsulfonyl)piperidine-4-carboxylate → HCID 15020362, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl 1-(phenylsulfonyl)piperidine-4-carboxylate | HCID 257103 | — |
| Reactant | HCID 178419651 | HCID 178419651 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 15020362 | HCID 15020362 | 29.8% |
Reaction Steps
To a solution of 25.1 g (0.085 mole) of 1-(phenylsulfonyl) -4-piperidine-carboxylic acid, ethyl ester in 500 ml of dry tetrahydrofuran cooled to 0° C. and under an atmosphere of nitrogen, was added 95 ml of a 2 molar solution(0.19 mole) of cyclohexylmagnesium bromide in ether. The mixture was stirred for 2 hr at ambient temperature and then was quenched on an icy solution of ammonium chloride. The mixture was extracted with methylene chloride. The methylene chloride solution was dried over magnesium sulfate, and the solvent was removed in vacuo to give a semisolid material. This was recrystallized from ethanol to give 8.50 g (29.8% yield) of title compound as a white, crystalline solid, m.p. 141°-143° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04950674 |
| Source dataset | uspto-grants-1990_08 |
| ORD ID | ord-0953e8c4a90943948f3f283986eef034 |
| Source note | uspto-grants-1990_08 |