Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Lithium Chloride | HCID 433294 | — |
| Reactant | 4-Iodobenzyl bromide | HCID 954258 | — |
| Reactant | Diethyl 2-(4-bromobenzyl)malonate | HCID 10860456 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 70976335 | HCID 70976335 | 84% |
Reaction Steps
A mixed liquid containing diethyl 4-bromobenzylmalonate (9.88 g, 30.0 mmol) and anhydrous N,N-dimethylformamide (12.0 mL) was added gradually at 0° C. to a mixed liquid containing sodium hydride (62 wt % in oil, 1.74 g, 45 mmol) and anhydrous N,N-dimethylformamide (18.0 mL). Following stirring of the resulting mixed liquid at this temperature for 30 minutes, a mixed liquid containing 4-iodobenzyl bromide (11.6 g, 39.0 mmol) and anhydrous N,N-dimethylformamide (30 mL) was added. The resulting mixed liquid was stirred at room temperature for 3 hours, and a saturated aqueous solution of ammonium chloride was then added to halt the reaction. The organic layer was separated from the mixed liquid, and the water layer was extracted with ethyl acetate. The thus obtained organic layer was washed with a saturated saline solution and then dried using anhydrous magnesium sulfate. The organic layer was filtered, the filtrate was concentrated under reduced pressure, to the thus obtained residue were added lithium chloride (5.09 g, 120 mmol), water (1.08 mL) and N,N-dimethylformamide (100 mL), and the resulting mixture was heated for 12 hours at 160° C. The thus obtained mixed liquid was cooled to room temperature, water (100 mL) was added, and the mixture was extracted with ethyl acetate. The thus obtained organic layer was dried using anhydrous magnesium sulfate and filtered. The filtrate was concentrated under reduced pressure, and the resulting residue was purified by silica gel column chromatography (hexane:ethyl acetate=70:1), yielding the title compound (4h) (11.9 g, 25.2 mmol) as a yellow liquid in a yield of 84%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09051246B2 |
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| Source dataset | uspto-grants-2015_06 |
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| ORD ID | ord-93e8642c16774cf4aaceb413b310bbff |
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| Source note | uspto-grants-2015_06 |
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