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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 443318Generated: October 30, 2026

Diethyl Malonate → 2H-1-Benzopyran-3-carboxylic acid, 7-(diethylamino)-2-oxo-, ethyl ester

https://huagongshe.com/reaction/443318

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl MalonateHCID 7761—
ReactantPiperidineHCID 8082—
Reactant4-(Diethylamino)-2-hydroxybenzaldehydeHCID 87293—
SolventEthanolHCID 702—
Product2H-1-Benzopyran-3-carboxylic acid, 7-(diethylamino)-2-oxo-, ethyl esterHCID 120014—

Reaction Steps

--A solution of 4-diethylamino-2-hydroxy-benzaldehyde (29.8 g, 154 mmol) and diethyl malonate (23.8 ml, 157 mmol) in ethanol (185 ml) was treated with piperidine (1.37 ml, 13.9 mmol) and heated under reflux for 4 h. The solution was allowed to cools then concentrated under reduced pressure to approx. half-volume diluted with ether and washed with water, dilute aq. NaOH and water, dried and evaporated under reduced pressure. Trituration of the residue with EtOH (approx. 15 ml) gave yellow crystals which were recrystallised from EtOAc-light petroleum to give the ester 1 as bright yellow prisms (18 the m.p. 76-77° C. A sample recrystallised a second time had m.p. 77-78° C. (Found: C, 66.4; H, 6.7g N, 4.8. C16H9NO4 requires C, 66.4; H, 6.6; N, 4.8%). The discrepancy with the m.p. (87° C.) reported by Kendal et al. (GB 867,592), together with the sharp m.p. and satisfactory analytical result for the present sample suggests that the digits of the reported value may accidently have been transposed.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05898069
Source datasetuspto-grants-1999_04
ORD IDord-a410396d14ec4a91aba2151f2b2245a8
Source noteuspto-grants-1999_04