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Carbon Disulfide → HCID 58319006、化合物

HRID 1750046
ノート
印刷プレビュー

反応式

HRID 1750046 の反応式
[CH3:1][O:2][C:3]1[CH:4]=[C:5]([CH2:11][CH2:12][NH2:13])[CH:6]=[C:7]([O:9][CH3:10])[CH:8]=1.C(N(CC)CC)C.[C:21](=S)=[S:22].S(Cl)(C1C=CC(C)=CC=1)(=O)=O>C1COCC1>[N:13]([CH2:12][CH2:11][C:5]1[CH:6]=[C:7]([O:9][CH3:10])[CH:8]=[C:3]([O:2][CH3:1])[CH:4]=1)=[C:21]=[S:22]
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 6348Carbon DisulfideHCID 73974-Toluenesulfonyl chlorideHCID 8471TriethylamineHCID 1378573,5-Dimethoxyphenethylamine

生成物 1

HCID 58319006HCID 58319006、化合物収率 100%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒2 回

実験手順

To a solution of 1.0 mL (1.0 g, 5.5 mmol) of 2-(3,5-dimethoxyphenyl)ethanamine (8) in 30 mL of THF was added dropwise 2.5 mL (1.8 g, 18.2 mmol) of triethylamine at 0° C. After stirring for 5 min, a solution of 420 mg (5.52 mmol) of carbon disulfide in 5 mL of THF was added dropwise at 0° C. The resulting solution was slowly warmed to room temperature, stirred for 1.5 h and then cooled to 0° C. To the reaction mixture was added 1.16 g (6.07 mmol) of tosyl chloride in one portion and solution stirred at room temperature for an additional hour. The reaction was quenched by slowly adding 30 mL of saturated NH4Cl(aq). The layers were separated and the aqueous phase was extracted once with ethyl acetate. The combined organic layers were dried (Na2SO4) and concentrated in vacuo. The residue was taken up in methylene chloride and filtered through a plug of silica gel (eluted with methylene chloride) and concentrated in vacuo to afford 1.2 g (100%) of 9 as a colorless oil: 1H NMR (400 MHz, CDCl3) δ 6.37 (s, 3H), 3.80 (s, 6H), 3.71 (t, J=7.0 Hz, 2H), 2.92 (t, J=7.0 Hz, 2H).

後処理

  1. stirringstirred for 1.5 h
  2. temperaturecooled to 0° C
  3. stirringstirred at room temperature for an additional hour
  4. customThe reaction was quenched
  5. additionby slowly adding 30 mL of saturated NH4Cl(aq)
  6. customThe layers were separated
  7. extractionthe aqueous phase was extracted once with ethyl acetate
  8. dry with materialThe combined organic layers were dried (Na2SO4)
  9. concentrationconcentrated in vacuo
  10. filtrationfiltered through a plug of silica gel (eluted with methylene chloride)
  11. concentrationconcentrated in vacuo

出典と根拠

ORDレコード
ord-a3c233ea96d04c16b9b234f638cfe751
出典データセット
uspto-grants-2015_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09156836B2

反応ノート

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