Sodium Chloride → Methyl 3-isopropoxy-4-(methylthio)benzoate

HRID 1940352

反応式

HRID 1940352 の反応式
[CH:1]([O:4][C:5]1[CH:6]=[C:7]([CH:12]=[CH:13][C:14]=1[N+]([O-])=O)[C:8]([O:10][CH3:11])=[O:9])([CH3:3])[CH3:2].[CH3:18][S-:19].[Na+].[Cl-].[Na+]>CN1CCN(C)C1=O.O>[CH:1]([O:4][C:5]1[CH:6]=[C:7]([CH:12]=[CH:13][C:14]=1[S:19][CH3:18])[C:8]([O:10][CH3:11])=[O:9])([CH3:3])[CH3:2]

参加物

6

反応物 3

HCID 5234Sodium ChlorideHCID 4378561Sodium methanethiolateHCID 21187964Methyl 3-isopropoxy-4-nitrobenzoate

生成物 1

HCID 21187888Methyl 3-isopropoxy-4-(methylthio)benzoate収率 69.9%

試薬・触媒・溶媒 2

HCID 962Water溶媒HCID 66611,3-Dimethyl-2-imidazolidinone溶媒

実験手順

A solution of methyl 3-isopropoxy-4-nitrobenzoate (5.7 g) in N,N'-dimethylimidazolidinone (35 mL) is treated with sodium thiomethoxide (2 g), and the mixture is stirred at room temperature for 4 hours. The mixture is then diluted with water (250 mL) containing sodium chloride (47 g), and is extracted with ethyl acetate (2×100 mL). The combined organic extracts are washed with brine (100 mL), dried over magnesium sulfate and evaporated in vacuo, to give a brown oil. The oil is subjected to flash chromatography, eluting with a 1.9 v/v mixture of diethyl ether and pentane, to give methyl 3-isopropoxy-4-(methylthio)benzoate (4.0 g), in the form of a cream solid, m.p. 41°-43° C.

後処理

  1. extractionis extracted with ethyl acetate (2×100 mL)
  2. washThe combined organic extracts are washed with brine (100 mL)
  3. dry with materialdried over magnesium sulfate
  4. customevaporated in vacuo
  5. customto give a brown oil
  6. washeluting with a 1.9 v/v mixture of diethyl ether and pentane

出典と根拠

ORDレコード
ord-3fc992e15eed440599bb12d816de2c57
出典データセット
uspto-grants-1997_12
特許番号
US05698711

関連ノート

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