HuagongsheHuagongshe Chemistry Print Report · For research reference only
Cyclohexane → Dibenzhydryl carboxymethylsuccinate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Cyclohexane | HCID 8078 | — |
| Reactant | Trityl acetate | HCID 621194 | — |
| Reactant | Lithium diisopropylamide | HCID 2724682 | — |
| Reactant | Dibenzhydryl maleate | HCID 67644151 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Water | HCID 962 | — |
| Product | Dibenzhydryl carboxymethylsuccinate | HCID 19073626 | 29% |
Reaction Steps
The reaction product obtained by conducting the Michael-addition reaction in the same manner as in Example 116 using 5.7 ml of a 1.5M cyclohexane solution of lithium diisopropylamide, 2.6 g of trityl acetate and 3.2 g of dibenzhydryl maleate, was dissolved in a liquid mixture of 20 ml of acetic acid and 5 ml of water, and the solution was left to stand at room temperature overnight and then evaporated to dryness under reduced pressure. The residue was subjected to silica gel column chromatography (chloroform/methanol=100/1→10/1) to obtain 1.05 g (yield: 29%) of the above-identified compound as white crystalline powder having a melting point of from 105° to 106° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05616803 |
| Source dataset | uspto-grants-1997_04 |
| ORD ID | ord-108a59315e044653b584b263eaa291a3 |
| Source note | uspto-grants-1997_04 |