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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1637681Generated: November 2, 2026

Water → HCID 70299656, compound

https://huagongshe.com/reaction/1637681

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTolueneHCID 1140—
ReactantSodium HydroxideHCID 14798—
Reactant2-Ethylpropanedioyl dichlorideHCID 10920924—
ReactantHCID 12412218HCID 12412218—
ProductHCID 70299656HCID 7029965695%

Reaction Steps

In a 100 ml roundbottom flask equipped with magnetical stirring, thermometer and addition funnel, 5,6,7,12-tetrahydrodibenzo[b,g]azocine (2.1 g, 0.01 mol, prepared in a similar way as described in Chem. Pharm. Bull 26, (1978), 942) was dissolved in dry toluene (60 ml) and ethyl malonyl chloride (2.0 g, 0.013 mol) was slowly added. The reaction mixture was heated at reflux temperature for 2 h and then allowed to cool to room temperature. Under stirring, 0.2N NaOH (5 ml) and water (60 ml) were added. More toluene was added (100 ml) and the phases were separated. The organic phase was washed with water (3×75 ml) and brine (75 ml). After drying (MgSO4), the organic phase was evaporated in vacuo affording 3.1 g (95%) of 3-(6,7-dihydro-5H-dibenzo[b,g]azocin-1 2-yl)-3-oxopropionic acid ethyl ester as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06043239
Source datasetuspto-grants-2000_03
ORD IDord-85d85872c6a54d33ac032f90e146c3cd
Source noteuspto-grants-2000_03