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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1003737Generated: October 31, 2026

2-Chlorobenzaldehyde → HCID 54282972, compound

https://huagongshe.com/reaction/1003737

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-ChlorobenzaldehydeHCID 6996—
ReactantPiperidineHCID 8082—
ReactantHCID 15428864HCID 15428864—
CatalystPiperidine, acetateHCID 9793820—
SolventIsopropanolHCID 3776—
ProductHCID 54282972HCID 5428297283%

Reaction Steps

10 g (33 millimoles) of ethyl-4-(2-iodoethoxy)-acetoacetate (XIII) and 4.64 g (33 millimoles) of 2-chloro-benzaldehyde (V) are reacted in 100 ml of isopropanol in the presence of a piperidine acetate catalyst [0.28 g (3.3 millimoles) of piperidine+0.198 g (3.3 millimoles) of acetic acid] at room temperature for 10 hours. The reaction mixture is evaporated, the residual oil dissolved in dichloro methane, washed with water and dried. The organic phase is evaporated in vacuo. Thus 11.55 g of the desired product are obtained in the form of a reddish brown oil, yield 83%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06046337
Source datasetuspto-grants-2000_04
ORD IDord-b7f453c806044400ada821e59cc902a5
Source noteuspto-grants-2000_04