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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 234676Generated: October 31, 2026

Water → HCID 70299656, compound

https://huagongshe.com/reaction/234676

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-12-yl)-3-oxopropionic acid ethyl ester as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05595989
Source datasetuspto-grants-1997_01
ORD IDord-3f70980e7c6d47e1a42e942acfe00ea5
Source noteuspto-grants-1997_01