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Hydrochloric Acid → HCID 178439097、化合物

HRID 1003983
ノート
印刷プレビュー

反応式

HRID 1003983 の反応式
[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]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 313Hydrochloric AcidHCID 702EthanolHCID 1382224-Isopropylphenylacetonitrile

生成物 1

HCID 178439097HCID 178439097、化合物収率 84%

試薬・触媒・溶媒 1

HCID 3283Diethyl Ether溶媒

反応条件

温度
0 °C

実験手順

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.

後処理

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

出典と根拠

ORDレコード
ord-0018fd886d444b23895bad42fb77072b
出典データセット
uspto-grants-2000_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06048862

反応ノート

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このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート