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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoromethanesulfonic anhydride | HCID 67749 | — |
| Reactant | Sodium Perchlorate | HCID 522606 | — |
| Reactant | 2-[1-Hydroxy-6'-(1-hydroxypentyl)-benzyl]pyridine | HCID 86749805 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | 6-Butylbenzo[b]quinolizinium perchlorate | HCID 19047476 | 11% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05554620 |
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| Source dataset | uspto-grants-1996_09 |
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| ORD ID | ord-049a5aa348bd45bf93c824cd8c0d8432 |
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| Source note | uspto-grants-1996_09 |
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