Hydrochloric Acid → 1-Propanone, 3-(1H-imidazol-1-yl)-1-(2-naphthalenyl)-, monohydrochloride

HRID 847719Notes

Reaction equation

HRID 847719 reaction equation
[ClH:1].[CH:2]1[C:11]2[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=2)[CH:5]=[CH:4][C:3]=1[C:12]([CH2:14][CH2:15][N:16]1[CH:20]=[CH:19][N:18]=[CH:17]1)=[O:13]>C1C=CC=CC=1>[ClH:1].[CH:2]1[C:11]2[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=2)[CH:5]=[CH:4][C:3]=1[C:12]([CH2:14][CH2:15][N:16]1[CH:20]=[CH:19][N:18]=[CH:17]1)=[O:13]

Participants

4

Reactant 2

HCID 313Hydrochloric AcidHCID 3058924HCID 3058924, compound

Product 1

HCID 30589231-Propanone, 3-(1H-imidazol-1-yl)-1-(2-naphthalenyl)-, monohydrochloride

Reagents, catalysts & solvents 1

HCID 241BenzeneSolvent

Procedure

Ethereal hydrogen chloride is added dropwise to a solution of 1.0 g 1-[2-(2-naphthoyl)ethyl]imidazole in 100 ml anhydrous benzene until precipitation is complete. The product is filtered, washed with ether, air dried and recrystallized from methanol/acetone to yield 1-[2-(2-naphthoyl)ethyl]imidazole hydrochloride, m.p. 182.5°-186° C.

Workup

  1. filtrationThe product is filtered
  2. washwashed with ether, air
  3. customdried
  4. customrecrystallized from methanol/acetone

Sources & evidence

ORD record
ord-8c4a0d0dbddd4b87ad44a50ae0c0a067
Source dataset
uspto-grants-1981_10
Patent number
US04293561

Reaction notes

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