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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 66164Generated: October 25, 2026

Methanesulfonic Acid → Methanesulfonate

https://huagongshe.com/reaction/66164

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonic AcidHCID 6395—
ReactantN-MethylcyclohexylamineHCID 7514—
Reactant2-(2-Ethoxy-2-phenyl-ethenyl)-1-pyrroline tetrafluoroborateHCID 86736214—
ProductMethanesulfonateHCID 85257—
Product2-[2-(N-methyl-cyclohexylamino)-phenylethenyl]-1-pyrroline-HCID 53716585—

Reaction Steps

Crude 2-[2-(N-methylcyclohexylamino)-phenylethenyl]-1-pyrroline is produced by heating the solution of 9.1 g (0.03 mole) of 2-(2-ethoxy-2-phenyl-ethenyl)-1-pyrroline-tetrafluoroborate in 20 ml of N-methyl-cyclohexylamine for 2 hours at 100°, and processing the reaction mixture analogously to Example 1. By addition of 2.8 g of methanesulphonic acid to the solution of the crude base in isopropanol, evaporation of this solution in the rotary evaporator and recrystallisation of the residue from ethyl acetate, there is obtained 2-[2-(N-methyl-cyclohexylamino)-phenylethenyl]-1-pyrroline-(1:1)-methanesulphonate, m.p. 163°-164°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04130652
Source datasetuspto-grants-1978_12
ORD IDord-e6a628c77d5e4abbaff5f78e9eabc531
Source noteuspto-grants-1978_12