Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Exalamide | HCID 3316 | — |
| Reactant | Triethyloxonium tetrafluoroborate | HCID 2723982 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 12254260 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03987160 |
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| Source dataset | uspto-grants-1976_10 |
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| ORD ID | ord-cd77abc13c7a4f1e8d4f435e89bdf3d7 |
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| Source note | uspto-grants-1976_10 |
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