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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 275646Generated: October 31, 2026

Water → HCID 54264222, compound

https://huagongshe.com/reaction/275646

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantDimethylformamideHCID 6228—
ReactantAllyl bromideHCID 7841—
ReactantTriethylamineHCID 8471—
ReactantHCID 53821646HCID 53821646—
ProductHCID 54264222HCID 54264222—
ProductHCID 54416959HCID 54416959—

Reaction Steps

10 g of diethyl 4-aminobenzylacetamidomalonate dissolved in 150 ml of DMF are placed in a three-necked flask which is surmounted with a dropping funnel and maintained under a nitrogen atmosphere. 6.57 ml of allyl bromide, and then 10.76 ml of triethylamine, are added slowly, at room temperature and while stirring. After stirring for 19 h, a further 1.31 ml of allylbromide and 2.15 ml of triethylamine are then added and the mixture is stirred for 26 h. The reaction medium is poured onto 1.5 l of distilled water and this mixture is extracted with 1 l of ethyl acetate. The aqueous phase is separated off after settling and washed with 2 times 500 ml of ethyl acetate. The organic phases are combined, washed with 500 ml of distilled water and then with 500 ml of water which is saturated with sodium chloride, separated off, dried over magnesium sulphate, filtered and then concentrated to dryness in order to yield a chestnut oil; this oil is purified by flash chromatography (eluant, CH2Cl290/AcOEt 10) in order to yield 6.66 g of diethyl 4-diallylaminobenzylacetamidomalonate in the form of a beige solid which melts at 94-96° C. (Rf=0.6, AcOEt 50/cyclohexane 50) and 3.49 g of diethyl 4-allylaminobenzylacetamidomalonate in the form of a beige solid which melts at 104-106° C. (Rf0.45 AcOEt 50/cyclohexane 50).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06352839B1
Source datasetuspto-grants-2002_03
ORD IDord-86df17c6bb4741a88a27b74fcbf1ebf9
Source noteuspto-grants-2002_03