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Isopropylamine → 4-(4-methoxyphenyl)-N-(1-methylethyl)butylamine

HRID 2417991
ノート
印刷プレビュー

反応式

HRID 2417991 の反応式
[CH3:1][O:2][C:3]1[CH:8]=[CH:7][C:6]([CH2:9][CH2:10][CH2:11][CH2:12]Br)=[CH:5][CH:4]=1.[CH:14]([NH2:17])([CH3:16])[CH3:15]>>[CH3:1][O:2][C:3]1[CH:8]=[CH:7][C:6]([CH2:9][CH2:10][CH2:11][CH2:12][NH:17][CH:14]([CH3:16])[CH3:15])=[CH:5][CH:4]=1
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

3

反応物 2

HCID 6363IsopropylamineHCID 5781911-(4-Bromobutyl)-4-methoxybenzene

生成物 1

HCID 204469294-(4-methoxyphenyl)-N-(1-methylethyl)butylamine

反応条件

温度
100 °C

実験手順

A solution of (50 ml) isopropylamine and 4-(4-methoxyphenyl)butyl bromide (13.7 g) in a glass lined vessel was heated under nitrogen (initial pressure, 500 psi) for 12 hours at 100° C. The solvent was removed in vacuo and water (200 ml) was added to the residue. The solution was acidified with concentrated hydrochloric acid and the solution was extracted with ether. The extract was dried over potassium carbonate and the solvent was removed in vacuo. The residue, 4-(4-methoxyphenyl)-N-(1-methylethyl)butylamine, weighed 9.3 g (75%). The identity and purity (94.8%) of the product was determined by mass spectrum and gas chromatography.

後処理

  • customThe solvent was removed in vacuo and water (200 ml)
  • additionwas added to the residue
  • extractionthe solution was extracted with ether
  • dry with materialThe extract was dried over potassium carbonate
  • customthe solvent was removed in vacuo
  • 出典と根拠

    ORDレコード
    ord-70a8b85604b7449ebbe788cd8acdafb8
    出典データセット
    uspto-grants-1984_09
    DOI
    10.6084/m9.figshare.5104873.v1
    特許番号
    US04471116

    反応ノート

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