HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1866086Generated: November 2, 2026
Hydrochloric Acid → Dimethyl(2-chloro-4-cyanophenyl)malonate
https://huagongshe.com/reaction/1866086
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Diethyl Malonate | HCID 7761 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 4-Bromo-3-chlorobenzonitrile | HCID 16659395 | — |
| Catalyst | copper(I) bromide | HCID 24593 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | Dimethyl(2-chloro-4-cyanophenyl)malonate | HCID 57977442 | 94.8% |
Reaction Steps
7.6 g (0.191 mol) of 60% strength sodium hydride in paraffin oil were initially charged in 300 ml of dioxane. At from 55° C. to 60° C., 22.9 g (0.173 mol) of diethyl malonate were added dropwise, and the mixture was stirred at 50° C. for 1-2 hours. 9.9-g (0.069 mol) of copper(1) bromide were added. At 80° C., 15 g (0.069 mol) of 3-chloro-4-bromobenzonitrile were then added dropwise, and the mixture was subsequently stirred at 100° C. for 14 hours. The reaction mixture was then cooled and acidified by dropwise addition of concentrated hydrochloric acid at from 15° C. to 20° C. Water was added, the mixture was extracted with dichloromethane, the organic phase was dried over sodium sulphate and the solvent was removed. The residue was distilled at 1 mbar, giving 17.5 g of dimethyl(2-chloro-4-cyanophenyl)malonate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07629294B2 |
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| Source dataset | uspto-grants-2009_12 |
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| ORD ID | ord-eb4ad380124f472fbedda80532c3e92a |
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| Source note | uspto-grants-2009_12 |
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