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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 492656Generated: October 31, 2026

Diethyl Malonate → Diethyl 2-(benzyloxyhexyl)malonate

https://huagongshe.com/reaction/492656

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl MalonateHCID 7761—
ReactantSodiumHCID 5360545—
ReactantHCID 15890138HCID 15890138—
SolventEthanolHCID 702—
ProductDiethyl 2-(benzyloxyhexyl)malonateHCID 1038323968.2%

Reaction Steps

To sodium metal (1.32 g, 0.0573 mol) dissolved in dry ethanol (150 ml) under argon at room temperature was added diethyl malonate (14.13 g, 0.088 mol) over a period of 10 minutes and the solution left for 2 hours. B1 (10.0 g 0.044 mol) was then added dropwise over 2 hours and this solution heated at reflux overnight. Excess salts were quenched by the addition of 50 ml of water and the total solvent volume reduced to 50-100 ml. Diethyl ether (100 ml) and water (50 ml) were added and the aqueous layer extracted 3 times with diethyl ether. The organic fractions were combined, dried (K2CO3), and the solvent removed to yield the crude product as a yellow oil. Distillation of the oil (0.5 mBar, 220° C.) gave the title compound (10.52 g, 68%) as a colourless viscous oil. δH (CDCl3) 1.32 (6H, t, Me), 1.43 (6H, br s, (CH2)3CH2CH), 1.69 (2H, p, CH2CH2O), 1.99 (2H, q, CH2CH), 3.39 (1H, t, CH), 3.53 (2H, t, CH2OCH2Ph), 4.25, 4.28 (4H, 2×q, OCH2Me), 4.57 (2H, s, CH2Ph), 7.3-7.4 (5H, m, Ph). δC (CDCl3) 13.9 (2 C, Me), 25.7 (1 C, CH2(CH2)2CH), 27.1 (1 C, CH2(CH2)2O), 28.5 (1 C, CH2CH2CH), 28.9 (1 C, CH2CH2O), 29.5 (1 C, CH2CH), 51.8 (CHCO2Et), 61.0 (2C, OCH2Me), 70.1, 72.7 (2C, CH2OCH2), 127.3 (1C, CH(CH)2C), 127.4 (2C, CGC), 128.1 (2C, CHCHC), 138.5 (1C, CCH2O) 169.3 (2C, CO2).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07531676B2
Source datasetuspto-grants-2009_05
ORD IDord-1b17d947805948688cbaa2a41f8a0f65
Source noteuspto-grants-2009_05