HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 1-[3,3-Di(ethoxycarbonyl)propyl]-4-methoxymethylbenzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Diethyl Malonate | HCID 7761 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | 1-(2-Bromoethyl)-4-(methoxymethyl)benzene | HCID 20197428 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 1-[3,3-Di(ethoxycarbonyl)propyl]-4-methoxymethylbenzene | HCID 20197602 | — |
Reaction Steps
Diethyl malonate (0.32 g) is added to a solution of 0.05 g sodium in 10 ml of methanol. The 1-(methoxymethyl)-4-(2-bromoethyl)benzene (13) (0.5 g) is then added and allowed to react for 8 h. The solution is neutralized with methanolic HCl and is extracted with ether. The ether extract is dried over Na2SO4, and evaporated to yield 1-[3,3-di(ethoxycarbonyl)propyl]-4-methoxymethylbenzene (14). The methyl group is removed by treatment with aqueous HBr in acetic acid, followed by neutralization with aqueous NaOH and extraction with ether. The ether extract is dried over Na2SO4, and evaporated to yield 1-[3,3-di(ethoxycarbonyl)propyl]-4-hydroxymethylbenzene (4).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04595690 |
| Source dataset | uspto-grants-1986_06 |
| ORD ID | ord-8a865185406345d196afb0df92b2a7c3 |
| Source note | uspto-grants-1986_06 |