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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 742473Generated: October 30, 2026

Trifluoromethanesulfonic anhydride → 6-Butylbenzo[b]quinolizinium perchlorate

https://huagongshe.com/reaction/742473

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoromethanesulfonic anhydrideHCID 67749—
ReactantSodium PerchlorateHCID 522606—
Reactant2-[1-Hydroxy-6'-(1-hydroxypentyl)-benzyl]pyridineHCID 86749805—
SolventBenzeneHCID 241—
Product6-Butylbenzo[b]quinolizinium perchlorateHCID 1904747611%

Reaction Steps

To a refluxing solution of 11.1 g (0.04 mol) of 2-[1-hydroxy-6'-(1-hydroxypentyl)-benzyl]pyridine in 250 mL of benzene was added 23.9 mL (0.14 mol) of triflic anhydride in 5 min, the mixture was heated for 65 min and then cooled. The reaction mixture was concentrated in vacuo, the residual oil was triturated in ether and decanted. The oil was chromatographed on silica (ethyl acetate/methylene chloride, 1:1 ) to afford an oil, which was treated with sodium perchlorate solution. The salt was triturated in hot water, decanted, and the residue crystallized on cooling. The above solid was crystallized (2×) from ethyl acetate/methylene chloride to afford 1.5 g (11%) of 6-butylbenzo[b]quinolizinium perchlorate (Formula II: R1 =R7 =H; R2 =n-butyl; X- =ClO4-), as a pale solid, m.p. 174°-177° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05554620
Source datasetuspto-grants-1996_09
ORD IDord-049a5aa348bd45bf93c824cd8c0d8432
Source noteuspto-grants-1996_09