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Water → Methyl 2-[(3,4-dimethoxyphenyl)thio]-3-(3-phenylpropyl-1-yl)-1-cyclopentenecarboxylate

HRID 1107128
ノート
印刷プレビュー

反応式

HRID 1107128 の反応式
Cl[C:2]1[C:6](=[CH:7][CH2:8][CH2:9][C:10]2[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=2)[CH2:5][CH2:4][C:3]=1[C:16]([O:18][CH3:19])=[O:17].[CH3:20][O:21][C:22]1[CH:23]=[C:24]([SH:30])[CH:25]=[CH:26][C:27]=1[O:28][CH3:29].C(=O)([O-])[O-].[K+].[K+].O>CO>[CH3:20][O:21][C:22]1[CH:23]=[C:24]([S:30][C:2]2[C:6](=[CH:7][CH2:8][CH2:9][C:10]3[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=3)[CH2:5][CH2:4][C:3]=2[C:16]([O:18][CH3:19])=[O:17])[CH:25]=[CH:26][C:27]=1[O:28][CH3:29]
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 962WaterHCID 11430Potassium CarbonateHCID 1365393,4-Dimethoxybenzene-1-thiolHCID 69907722Methyl 2-chloro-3-(3-phenylpropyl-1-yl)-1-cyclopentenecarboxylate

生成物 1

HCID 69907819Methyl 2-[(3,4-dimethoxyphenyl)thio]-3-(3-phenylpropyl-1-yl)-1-cyclopentenecarboxylate収率 58%

試薬・触媒・溶媒 1

HCID 887
Methanol
溶媒

実験手順

A mixture of Methyl 2-chloro-3-(3-phenylpropyl-1-yl)-1-cyclopentenecarboxylate (0.2 g, 0.72 mmol), 3,4-dimethoxythiophenol (0.12 g, 0.72 mmol) and potassium carbonate (0.1 g, 0.72 mmol) in methanol (20 mL) is heated under reflux for 6 hours. After standing at room temperature for 2 days, the mixture is heated under reflux for another 4 hours. The mixture is poured into water and is extracted with ether. The organic layer is washed with water and is dried over MgSO4. The solvent is removed in vacuo and the residue is chromatographed on silica gel (4:1 hexane:ethyl acetate) to provide methyl 2-[(3,4-dimethoxyphenyl)thio]-3-(3-phenylpropyl-1-yl)-1-cyclopentenecarboxylate (0.17 g, 58%): 1H-NMR (300 MHz, CDCl3) δ (TMS) 1.10-1.70 (m, 5H), 1.88-1.98 (m, 1H), 2.31-2.40 (t, 3H), 2.58-2.70 (t, 3H), 3.78 (s, 3H), 3.84 (s, 3H), 3.90 (s, 3H), 6.68-6.75 (d, 1H), 6.95-7.09 (m, 4H), 7.17-7.30 (m, 3H); MS (EI) m/e 412 (M+).

後処理

  1. temperatureis heated
  2. temperatureunder reflux for 6 hours
  3. temperaturethe mixture is heated
  4. temperatureunder reflux for another 4 hours
  5. extractionis extracted with ether
  6. washThe organic layer is washed with water
  7. dry with materialis dried over MgSO4
  8. customThe solvent is removed in vacuo
  9. customthe residue is chromatographed on silica gel (4:1 hexane:ethyl acetate)

出典と根拠

ORDレコード
ord-71ab7b2607e54d7094960a05325e3111
出典データセット
uspto-grants-2000_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06057369

反応ノート

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