Hydrochloric Acid → HCID 178439097, 화합물

HRID 1003983

반응식

HRID 1003983 반응식
[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]

참가 물질

5

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온도
0 °C

실험 절차

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.

후처리

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

출처 및 근거

ORD 기록
ord-0018fd886d444b23895bad42fb77072b
출처 데이터셋
uspto-grants-2000_04
특허 번호
US06048862

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