HuagongsheHuagongshe Chemistry Print Report · For research reference only
Butanedioic acid, 2-acetyl-, 1,4-diethyl ester → HCID 178470721, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Butanedioic acid, 2-acetyl-, 1,4-diethyl ester | HCID 66197 | — |
| Reactant | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| Reactant | HCID 178424562 | HCID 178424562 | — |
| Solvent | O-Xylene | HCID 7237 | — |
| Product | HCID 178470721 | HCID 178470721 | — |
Reaction Steps
Diethyl acetylsuccinate (0.3 mL) and a catalytic amount of 4-toluenesulfonic acid monohydrate were added to a solution of 4-mesityl-3-methyl-1H-5-pyrazoleamine (100 mg) of Reference Example 1 in xylene (5 mL). Under heating under reflux, the mixture was stirred for three hours while distilling water off with Dean-Stark. The reaction solution was cooled, water was added thereto. the mixture was extracted twice with ethyl acetate, and washed twice with an aqeous saturated solution of sodium bicarbonate. The organic layer was separated and dried over anhydrous magnesium sulfate. The solvent was evaporated, and the residue was purified by silica gel column chromatography, to give the title compound (200 mg) as a yellow amorphous material.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06995163B2 |
| Source dataset | uspto-grants-2006_02 |
| ORD ID | ord-36d3718327b04e97aa2dd146392959bb |
| Source note | uspto-grants-2006_02 |