HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diethyl methylmalonate → 2-Methyl-4-bromo-1-indanone ethylene ketal
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diethyl methylmalonate | HCID 11857 | — |
| Reactant | 2-Bromobenzyl bromide | HCID 76965 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| Reactant | 4-Bromo-2-methyl-1-indanone | HCID 10537152 | — |
| Reactant | Ethylorthoformate | HCID 53630039 | — |
| Solvent | Ethylene Glycol | HCID 174 | — |
| Product | 2-Methyl-4-bromo-1-indanone ethylene ketal | HCID 57214909 | — |
Reaction Steps
To a solution of 4.88 g of 2-methyl-4-bromo-1-indanone derived from 2-bromobenzyl bromide and diethyl methylmalonate in 12 ml of ethylene glycol was added 5.4 ml of ethyl orthoformate. After a catalytic amount of p-toluenesulfonic acid monohydrate was added, the mixture was stirred overnight at room temperature. The reaction mixture was poured into saturated aqueous sodium hydrogen carbonate and extracted with ether. After the organic layer was dried over magnesium sulfate, the solvent was removed by distillation under reduced pressure. The residual concentrate was purified by silica gel column chromatography to give 4.08 g of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05594081 |
| Source dataset | uspto-grants-1997_01 |
| ORD ID | ord-dc5a3af1c4ce494d946f803269e9b57f |
| Source note | uspto-grants-1997_01 |