HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diethyl methylmalonate → Diethyl 2-(4-bromobenzyl)malonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diethyl methylmalonate | HCID 11857 | — |
| Reactant | 4-Bromobenzyl bromide | HCID 68527 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Diethyl 2-(4-bromobenzyl)malonate | HCID 10860456 | 91.7% |
Reaction Steps
A solution of diethyl methylmalonate (87 g) in absolute ethanol (100 ml) was added to a pre-formed solution of sodium (11.5 g) in ethanol (400 ml) under argon. A hot solution of p-bromobenzylbromide (125 g) in absolute alcohol (200 ml) was added rapidly with vigorous stirring, which was continued for 3 days and the solid so formed was removed by filtration. The filtrate was evaporated and the residue dissolved in ethyl acetate (1 l), washed with brine (250 ml), dried (MgSO4) and evaporated. The residual oil was distilled under vacuum to give diethyl (4-bromophenyl)methylmalonate (150.7 g) b.p. 130-133/0.03 mm Hg; 1H NMR (d6-DMSO): 1.33 (t, 6H), 1.4 (s, 3H), 3.27 (s, 2H), 4.30 (q, 4H), 7.23 (d, 2H), 7.6 (d, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06258817B1 |
| Source dataset | uspto-grants-2001_07 |
| ORD ID | ord-0c22c41e7026463d98e7db5278c58230 |
| Source note | uspto-grants-2001_07 |