HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl 2-methyl-1-oxo-2,3-dihydro-1H-indene-2-carboxylate → Methyl 2-methyl-2,3-dihydro-1H-indene-2-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl 2-methyl-1-oxo-2,3-dihydro-1H-indene-2-carboxylate | HCID 12522314 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Sulfuric Acid | HCID 1118 | — |
| Product | Methyl 2-methyl-2,3-dihydro-1H-indene-2-carboxylate | HCID 57565328 | — |
Reaction Steps
A solution of the methyl 2-methyl-1-oxo-2,3-dihydro-1H-indene-2-carboxylate (2.04 g, 9.99 mmol) in glacial acetic acid (22 mL) and concentrated H2SO4 (2 mL) was hydrogenated on a Parr apparatus under 50 psi of hydrogen using 10% palladium on carbon (50% H2O, 0.200 g) as the catalyst. After 4 hours the reaction was filtered to remove the catalyst and washed 2× methanol, then concentrated to remove most of the acetic acid. The residue was neutralized using saturated Na2CO3 and the organics extracted twice with 25 mL ethyl acetate, then the combined organics washed with brine, dried (Na2SO4), filtered and concentrated to 2.0 g of methyl 2-methyl-2,3-dihydro-1H-indene-2-carboxylate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07939528B2 |
| Source dataset | uspto-grants-2011_05 |
| ORD ID | ord-51d3487e014240dba915a8efcdb4f4a2 |
| Source note | uspto-grants-2011_05 |