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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1731772Generated: October 31, 2026

Benzaldehyde → HCID 14010268, compound

https://huagongshe.com/reaction/1731772

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzaldehydeHCID 240—
ReactantTriethylamineHCID 8471—
Reactant87484-94-4HCID 14010266—
SolventBenzeneHCID 241—
ProductHCID 14010268HCID 1401026850%

Reaction Steps

A mixture of 4.0 g (0.02 mole) of 2-[N-[(dimethylamino)sulfonyl]amino]ethylamine hydrochloride and 2.0 g (0.02 mole) of benzaldehyde was stirred and treated immediately with 2.0 g (0.02 mole) of triethylamine, followed by the addition of 200 ml of dry benzene. The solution was heated to reflux employing a Dean-Stark apparatus. After 2 hr at reflux, the benzene solution was cooled and washed twice with 100 ml portions of water. The organic phase was separated, dried over magnesium sulfate, and concentrated under reduced pressure to an oil, which was dissolved in ether and treated with HCl gas to precipitate a yellowish solid. The product was collected by filtration, washed with ether and air dried to provide 2.4 g (50%) of product. The NMR spectrum was consistent with the assigned structure and the solid was used without additional purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04623652
Source datasetuspto-grants-1986_11
ORD IDord-5d7a066656ad4148b5dcf1a013b76652
Source noteuspto-grants-1986_11