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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1588044Generated: October 31, 2026

Chloroacetaldehyde → HCID 54283362, compound

https://huagongshe.com/reaction/1588044

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroacetaldehydeHCID 33—
ReactantPyridineHCID 1049—
ReactantDiethyl MalonateHCID 7761—
ReactantTetrahydrofuranHCID 8028—
CatalystTitanium TetrachlorideHCID 24193—
SolventWaterHCID 962—
SolventCarbon TetrachlorideHCID 5943—
ProductHCID 54283362HCID 5428336244%

Reaction Steps

A solution of titanium (IV) chloride (11 ml, 0.1M) in carbon tetrachloride (25 ml) was added dropwise to anhydrous tetrahydrofuran (200 ml) at 0° under nitrogen. On completion of the addition, diethyl malonate (7.6 ml, 50 mM) and anhydrous chloroacetaldehyde (5 g, 63 mM) were added, then a solution of pyridine (16 ml, 0.2M) in anhydrous tetrahydrofuan (35 ml) was added dropwise over 2 hours at 0°. On completion of the addition, the dark mixture was allowed to warm to room temperature, stirred at this temperature for 2 hours, then heated under reflux overnight. The reaction mixture was cooled, water (500 ml) added and the mixture extracted with diethyl ether (2×250 ml). The combined extracts were washed with water (500 ml), saturated sodium bicarbonate solution (500 ml) and brine (500 ml), dried (MgSO4) and evaporated to give a brown oil. Column chromatography of this oil on silica (eluent 1:1 hexane:dichloromethane) afforded the title compound as a pale yellow oil 4.9 g, 44%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05220024
Source datasetuspto-grants-1993_06
ORD IDord-03eb7fe84a754667b342ed7996b108c3
Source noteuspto-grants-1993_06