Hydrochloric Acid → HCID 178439097, compound

HRID 1740368Notes

Reaction equation

HRID 1740368 reaction equation
[CH:1]([C:4]1[CH:9]=[CH:8][C:7]([CH2:10][C:11]#[N:12])=[CH:6][CH:5]=1)([CH3:3])[CH3:2].C([OH:15])C.[ClH:16]>CCOCC>[ClH:16].[CH:1]([C:4]1[CH:5]=[CH:6][C:7]([CH2:10][C:11](=[NH:12])[OH:15])=[CH:8][CH:9]=1)([CH3:3])[CH3:2]

Participants

5

Conditions

Temperature
0 °C

Procedure

To a solution of 4-isopropylphenylacetonitrile (2 g, 12.5 mmol) in anhydrous ether (50 mL) was added absolute ethanol (0.5 g, 12.5 mmol) and an excess of HCl gas was passed into the solution with cooling in an ice bath. The resulting solution was allowed to stir at 0° C. for 1.5 hours and at room temperature overnight. The white solid was collected by filtration, washed with ether (2×20 mL) and dried to give 2.52 g (84%) of 4-isopropylphenylacetimidate hydrochloride as white crystals, mp 118-120° C. A solution of ethylenediamine (1.25 g, 20 mmol) in absolute ethanol (5 mL) was added to a solution of the imidate hydrochloride (2.5 g, 10 mmol) in absolute ethanol (15 mL) cooled at ice-bath temperature. After stirring at 0° C. for 1 hour, the solution was heated at reflux for 20 minutes. The solvent was evaporated and the oily residue was washed with water (2×3 mL) and extracted with methylene chloride (3×15 mL). The solution was dried (MgSO4), filtered and evaporated under reduced pressure to afford 2 g of the free base of the title compound. A solution of the free base in anhydrous ether was treated with dry HCl gas. The crude salt was collected and recrystallized from ethanol/ether to give 1.95 g (79%) of the title compound as a white solid. mp 176-178° C.; Anal. C13H18N2.HCl: C, H, N.

Workup

  1. temperaturewith cooling in an ice bath
  2. filtrationThe white solid was collected by filtration
  3. washwashed with ether (2×20 mL)
  4. customdried

Sources & evidence

ORD record
ord-ff80a60b2ae54d7e8d908991d0236edb
Source dataset
uspto-grants-1999_10
Patent number
US05969137

Reaction notes

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