HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Methylpiperazine → Cyclohexanecarboxylic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Methylpiperazine | HCID 53167 | — |
| Reactant | (-)-trans-1,2-Cyclohexanedicarboxylic Anhydride | HCID 12261141 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | Cyclohexanecarboxylic acid | HCID 7413 | — |
Reaction Steps
0.37 cm3 of N-methylpiperazine in solution in 5 cm3 of dioxane is added, under an argon atmosphere, to 0.50 g of (−)-trans-1,2-cyclohexanedicarboxylic anhydride in solution at −15° C. in 20 cm3 of dioxane. After 1.25 hours at 20° C., the reaction mixture is filtered, the solid is washed with 20 cm3 of diethyl ether, drained, and then dried under reduced pressure (2,7 kPa) at 20° C., to give 0.65 g of (1R,2R)-2-(4-methylpiperazin-1-yl)carbonyl]-1-cyclohexanecarboxylic acid in the form of a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07166594B2 |
| Source dataset | uspto-grants-2007_01 |
| ORD ID | ord-5074a2d56d3647d9ae62befe38ce5166 |
| Source note | uspto-grants-2007_01 |