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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 131116Generated: November 1, 2026

Diethyl Malonate → HCID 594682, compound

https://huagongshe.com/reaction/131116

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl MalonateHCID 7761—
ReactantHomoallyl bromideHCID 21241—
ReactantSodium hydrideHCID 24758—
SolventDimethylformamideHCID 6228—
ProductHCID 594682HCID 59468271%

Reaction Conditions

Temperature0 °C

Reaction Steps

A mixture of sodium hydride (60% in mineral oil, 435 mg, 10.87 mmol, 1.1 eq) in DMF (20 mL) was treated dropwise with diethyl malonate (1.5 mL, 9.88 mmol, 1.0 eq). The reaction mixture was then cooled to 0° C. and 4-bromo-1-butene (1.0 mL, 9.88 mmol, 1 eq) was added dropwise. The reaction mixture was warmed to rt, stirred for 3 days and then partitioned between ether and water. The layers were separated, the aqueous layer was extracted with ether (2×50 mL) and the combined organic phases were washed with water (2×) and brine, dried over MgSO4 and concentrated. Column chromatography (SiO2, 5% ether/heptane) gave C8.1 (1.51 g, 71% yield) as a colorless oil. 1H NMR (400 MHz, DMSO-d6): δ 5.77 (m, 1 H), 5.00 (m, 2 H), 4.13 (q, J=7.1 Hz, 4 H), 3.43 (t, J=7.4 Hz, 1 H), 2.02 (m, 2 H), 1.84 (m, 2 H), 1.17 (t, J=7.1 Hz, 6 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07384937B2
Source datasetuspto-grants-2008_06
ORD IDord-13ca2e55ae2c4f71b3b1daa42aa7af65
Source noteuspto-grants-2008_06