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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 46681Generated: October 30, 2026

Hydrochloric Acid → HCID 22809257, compound

https://huagongshe.com/reaction/46681

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTetrahydrofuranHCID 8028—
ReactantSodium HydroxideHCID 14798—
Reactant2,3,4,5-tetrahydro-2-methyl-5-phenyl-1H-pyrido[4,3-b]indoleHCID 746616—
SolventEthanolHCID 702—
SolventDiethyl EtherHCID 3283—
ProductHCID 22809257HCID 22809257—

Reaction Conditions

Temperature50 °C

Reaction Steps

To a solution of 180 ml 1 molar BH3 in THF (0.18 mole BH3) which was cooled in an ice bath, was added a solution of 7.9 grams 2,3,4,5-tetrahydro-2-methyl-5-phenyl-1H-pyrido[4,3-b]indole (0.03 mole) in 200 ml freshly chromatographed THF, dropwise with stirring over 30 minutes in a nitrogen atmosphere. The ice bath was then replaced with a heating mantle and the mixture was refluxed for 19 hours in the nitrogen atmosphere. The mixture was cooled and evaporated under vacuum to a clear gel. The gel was then refluxed in 75 ml of a 1:1 mixture of glacial acetic acid and 5 N HCl. A clear light brown solution was obtained after about 1/2 hour and refluxing was continued for a total of 1 hour. The resulting solution was cooled to about 50° C. and treated with 50% aqueous NaOH until basic, during which time the temperature rose to 80° C. The mixture was cooled again and a light purple oil was extracted into CHCl3. The mixture was again extracted with CHCl3, the extracts were combined and washed with saturated NaCl solution, then dried over Na2SO4. The CHCl3 was then evaporated under vacuum, leaving a purple oily residue which was taken up in about 50 ml diethyl ether and some ethanol. Ethereal HCl was added and 8.1 grams of pale greenish-white powder were obtained by filtration and drying. Recrystallization from methanol provided 6.2 grams of the title compound, m.p. 256°-258° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04174453
Source datasetuspto-grants-1979_11
ORD IDord-19c9324ecce347e69908f332cf586a42
Source noteuspto-grants-1979_11