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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1288263Generated: October 31, 2026

Exalamide → HCID 12254260, compound

https://huagongshe.com/reaction/1288263

Reaction equation

Participants

RoleNameHCIDCharge
ReactantExalamideHCID 3316—
ReactantTriethyloxonium tetrafluoroborateHCID 2723982—
SolventDichloromethaneHCID 6344—
ProductHCID 12254260HCID 12254260—

Reaction Steps

To a solution of 2-hexyloxybenzamide (64 g; prepared as described by E. M. Bavin, F. J. Macrae, D. E. Seymour and P. D. Waterhouse, J.Pharm.Pharmacol., 1952, 4, 872) in anhydrous methylene chloride (830 ml.) was added, dropwise during 10 minutes with stirring, a solution of triethyloxonium borofluoride (55.2 g.) in anhydrous methylene chloride (170 ml.). The solution was stirred for a further 105 minutes, and allowed to stand at room temperature for 2 days. The solution was concentrated to 350 ml., and anhydrous diethyl ether (1750 ml.) was added. The precipitated solid was filtered off and washed with anhydrous diethyl ether to give ethyl 2-hexyloxybenzimidate borofluoride (62 g.), m.p. 68°-70° C., which was pure enough to use for the next stage of the synthesis. A pure sample, m.p. 73°-74° C., was obtained by recrystallisation of an aliquot from a mixture of anhydrous methylene chloride and anhydrous diethyl ether.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03987160
Source datasetuspto-grants-1976_10
ORD IDord-cd77abc13c7a4f1e8d4f435e89bdf3d7
Source noteuspto-grants-1976_10