HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1290319Generated: October 25, 2026
Diethyl Malonate → Diethyl 2-(1-Bromo-2-naphthylmethyl)malonate
https://huagongshe.com/reaction/1290319
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diethyl Malonate | HCID 7761 | — |
| Reactant | 1-Bromo-2-(bromomethyl)naphthalene | HCID 37828 | — |
| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Diethyl 2-(1-Bromo-2-naphthylmethyl)malonate | HCID 14491492 | 95.6% |
Reaction Steps
To a solution of NaOEt prepared from 9.66 g of sodium and 210 mL of dry EtOH was added 63.76 mL of diethyl malonate and the reaction mixture refluxed for 2 h. To the resulting yellow solution was added in small portions 126 g of 1-bromo-2-bromomethylnaphthalene and the reaction mixture refluxed for 16 h. Distillation of ethanol from an oil bath (100°-110° C.) through a simple Claisen head gave a yellow suspension, to which was added 350 mL of CH2Cl2 and 350 mL of H2O. The aqueous layer was extracted twice with 120-mL portions of CH2Cl2, and the combined organic layer was washed three times with 100-mL portion of H2O, dried (MgSO4) and evaporated to give 152 g (95.6%) of the ester as a yellow solid, mp 60°-65° C. Recrystallization from acetic acid gave 137 g (86.2%) of the pure diester as a colorless solid, mp 77°-79° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05750767 |
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| Source dataset | uspto-grants-1998_05 |
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| ORD ID | ord-edce69a42435422ba59d585e8c0d274a |
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| Source note | uspto-grants-1998_05 |
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