HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 39200Generated: October 28, 2026
Methyl iodide → 1,3-Diethyl 2-(4-bromophenyl)-2-methylpropanedioate
https://huagongshe.com/reaction/39200
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Diethyl 4-bromophenylmalonate | HCID 10519382 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1,3-Diethyl 2-(4-bromophenyl)-2-methylpropanedioate | HCID 10616307 | 55% |
Reaction Steps
To a solution of diethyl 2-(4-bromophenyl)malonate (1.5 g, 4.8 mmol) in dry THF (5 mL) at 0° C. was added sodium hydride (380 mg, 9.5 mmol). After stirring for 30 minutes at 0° C., iodomethane (600 μL, 9.5 mmol) was added and the reaction was allowed to warm to room temperature. After stirring for 12 h at room temperature, the reaction was quenched with water (3 mL). The mixture was partitioned between 1 N HCl (10 mL) and dichloromethane (10 mL), and the organic layer was separated. The organic layer was washed with 1 N HCl (10 mL), dried over Na2SO4 and evaporated. The crude material was purified by silica gel chromatography, eluting with 0-20% ethyl acetate in hexanes, to give diethyl 2-(4-bromophenyl)-2-methylmalonate (850 mg, 55%) 1H NMR (400 MHz, DMSO-d6) δ 7.59-7.55 (m, 2H), 7.31-7.27 (m, 2H), 4.21-4.14 (m, 4H), 1.75 (s, 3H), 1.19-1.16 (m, 6H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08524767B2 |
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| Source dataset | uspto-grants-2013_09 |
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| ORD ID | ord-16879a0a0bc44b89958b8465a906fb28 |
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| Source note | uspto-grants-2013_09 |
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