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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1680664Generated: November 3, 2026

Sodium amide → HCID 54152167, compound

https://huagongshe.com/reaction/1680664

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium amideHCID 24533—
Reactant3-Chloro-N,N-dimethyl-1-propanamineHCID 66960—
Reactant10-MethoxyiminostilbeneHCID 78424—
ReactantChloroform methanolHCID 21584188—
SolventWaterHCID 962—
ProductHCID 54152167HCID 5415216792.8%

Reaction Steps

A 500 ml round bottom flask containing 9.87 g (0.044 moles) of 10-methoxy-5H-dibenz[b,f]azepine prepared in Example 3 and 13.9 g (0.088 moles) of 3-dimethylaminopropylchloride was evacuated for several days. Anhydrous toluene (250 ml) was added followed by 7.04 g (0.176 moles) of sodium amide. The heterogeneous solution was stirred at ambient temperature for a few minutes and then refluxed for 16 hours. After 16 hours of refluxing, tlc analysis of the reaction mixture (silica gel GF plates, methanol:chloroform 1:9; visualized under UV lamp and sulfuric acid-ceric sulfate spray) revealed that the reaction was complete and that no starting material remained. Enough water was added to slowly decompose the excess sodium amide. The dark-brown solution was placed in a 1 liter separatory funnel and extracted with four 250 ml portions of water. The organic phase was dried over anhydrous magnesium sulfate, charcoal was added and the mixture was filtered through a Celite pad. The filtrate was concentrated leaving a brown oil (12.6 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04275160
Source datasetuspto-grants-1981_06
ORD IDord-bc3a464ce9fd443190c8cb4d5e8e98ca
Source noteuspto-grants-1981_06