関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Dimethyl Sulfide | HCID 1068 | — |
| 反応物 | Dimethyl Sulfate | HCID 6497 | — |
| 反応物 | 2-Butanone, 1-(4-chlorophenoxy)-3,3-dimethyl- | HCID 90518 | — |
| 反応物 | Sodium Methoxide | HCID 10942334 | — |
| 溶媒 | Acetonitrile | HCID 6342 | — |
| 生成物 | 2-tert-Butyl-2-[(4-chlorophenoxy)methyl]oxirane | HCID 12763621 | 84% |
反応手順
A solution of 162 ml (2.2 moles) of dimethyl sulphide in 400 ml of absolute acetonitrile was added to a solution of 189 ml (2.0 moles) of dimethyl sulphate in 1,200 ml of absolute acetonitrile at room temperature. The reaction mixture was stirred overnight at room temperature. 118.8 g (2.2 moles) of sodium methylate were then added. The mixture was stirred for 30 minutes and a solution of 272 g (1.2 moles) of 1-(4-chlorophenoxy)-3,3-dimethyl-butan-2-one in 600 ml of absolute acetonitrile was then added dropwise in the course of 30 minutes. The reaction mixture was subsequently stirred overnight. It was then concentrated, the residue was partitioned between water and ethyl acetate, the organic phase was separated off, washed twice with water and once with saturated sodium chloride solution, dried over sodium sulphate and concentrated and the residue was distilled in vacuo. 242.4 g (84% of theory) of 2-(4-chlorophenoxymethyl)-2-tert.-butyl-oxirane of boiling point 115°-22° C./0.003 mm Hg column and of melting point 50°-52° C. were obtained.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US04723984 |
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| 出典データセット | uspto-grants-1988_02 |
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| ORD ID | ord-b9a65196066a45deb5cb3baa21f1de1c |
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| 出典メモ | uspto-grants-1988_02 |
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