HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1285402Generated: October 30, 2026
Ethanol → Diethyl methyl(3-methylbut-2-en-1-yl)propanedioate
https://huagongshe.com/reaction/1285402
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethanol | HCID 702 | — |
| Reactant | Diethyl methylmalonate | HCID 11857 | — |
| Reactant | 2-Butene, 1-bromo-3-methyl- | HCID 70092 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Product | Diethyl methyl(3-methylbut-2-en-1-yl)propanedioate | HCID 13080719 | — |
Reaction Steps
36.1 g of sodium (cut into small pieces) was introduced into a three-necked flask equipped with reflux condenser, dropping funnel, and agitator. To this mixture was added 800 ml of absolute ethanol so quickly that the solution continued to boil vigorously. The hot alcoholate solution was combined dropwise with 269.6 g of freshly distilled methylmalonic acid diethyl ester, the mixture was stirred for 1/2 hour at 60° C. and then 241.7 g of dimethylallyl bromide was also added dropwise thereto. After one hour of agitation under heating, the thus-precipitated sodium bromide was filtered off, the precipitate was washed, and the filtrate was concentrated. The remainder was taken up in ether, washed neutral with saturated sodium chloride solution, dried over magnesium sulfate, and concentrated on a forced circulation evaporator. The evaporation residue was fractionated on an oil pump, yielding 266 g of the title compound, bp7 97°-112° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04567195 |
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| Source dataset | uspto-grants-1986_01 |
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| ORD ID | ord-2a05371960d64f6dab0b1e21ed513966 |
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| Source note | uspto-grants-1986_01 |
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