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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1003736Generated: October 31, 2026

2-Chlorobenzaldehyde → HCID 54543583, compound

https://huagongshe.com/reaction/1003736

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-ChlorobenzaldehydeHCID 6996—
ReactantPiperidineHCID 8082—
ReactantHCID 15428861HCID 15428861—
CatalystPiperidine, acetateHCID 9793820—
SolventIsopropanolHCID 3776—
ProductHCID 54543583HCID 5454358397%

Reaction Steps

16.64 g (0.118 mole) of 2-chloro-benzaldehyde (V) and 24.7 g (0.118 mole) of ethyl-4-(2-chloroethoxy)-acetoacetate (IV) are reacted in 365 ml of isopropanol in the presence of a piperidine acetate catalyst [10 g (11.8 millimoles) of piperidine+0.7 g (11.8 millimoles) of acetic acid] at room temperature for 10 hours. The reaction mixture is evaporated, the residual oil is dissolved in dichloro methane, washed with water and dried. The organic phase is evaporated in vacuo. Thus 37.9 g of the desired product are obtained in the form of a yellow oil, yield 97%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06046337
Source datasetuspto-grants-2000_04
ORD IDord-8f53d5c582bb4f5aab61dedae0a15b06
Source noteuspto-grants-2000_04