HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 473352Generated: October 30, 2026
Ethyl Bromide → (Z)-2-(Ethoxymethylene)-4,4-dimethylpentanal
https://huagongshe.com/reaction/473352
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl Bromide | HCID 6332 | — |
| Reactant | Methyl formate | HCID 7865 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | 4,4-Dimethylpentanal | HCID 11062343 | — |
| Solvent | Benzene | HCID 241 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (Z)-2-(Ethoxymethylene)-4,4-dimethylpentanal | HCID 86627013 | — |
Reaction Steps
4,4-Dimethylpentanal (4.20 g, 36.8 mmol, Step 2) in 36 mL of THF was added over 4 hours by syringe pump to a solution of sodium methoxide, 25 wt. % in methanol (15.1 ml, 66.2 mmol), 15 mL of methanol, and methyl formate (166 ml, 2685 mmol). Following the addition, the reaction was diluted with benzene (50 mL) and DMF (40 mL). The solvents were distilled off at 90° C. leaving the DMF and residual benzene. Bromoethane (11.0 ml, 147 mmol) was added and the solution was heated at 40° C. for 48 hrs and then cooled. The solution was diluted with water, and the reaction was extracted with ether. The combined organic layers were washed with water, brine, and dried over magnesium sulfate, filtered and concentrated to afford the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08633315B2 |
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| Source dataset | uspto-grants-2014_01 |
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| ORD ID | ord-eb84180e3bfe45c0bacc1f37a160b4b3 |
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| Source note | uspto-grants-2014_01 |
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