関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Thioglycolic Acid | HCID 1133 | — |
| 反応物 | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| 反応物 | 2-[3,4-(Methylenedioxy)phenyl]-2-butanol | HCID 19001698 | — |
| 溶媒 | Benzene | HCID 241 | — |
| 生成物 | [{1-(1,3-Benzodioxol-5-yl)-1-methylpropyl}thio]acetic acid | HCID 14514927 | 35.4% |
反応手順
50 ml of benzene, 1.29 g of mercaptoacetic acid and a catalytic amount of p-toluenesulfonic acid monohydrate were added to 2.27 g of 2-(1,3-benzodioxol-5-yl)-2-butanol (crude oil). The obtained mixture was heated under reflux for 11 hours and cooled, followed by the addition of benzene. The obtained mixture was washed with water, followed by the addition of a 1N aqueous solution of sodium hydroxide. The alkaline layer was separated, washed with ethyl acetate, acidified with concentrated hydrochloric acid and extrated with chloroform. The organic layer was washed with water, dried over anhydrous magnesium sulfate and filtered. The filtrate was distilled to remove the solvent. The residue was purified by silica gel column chromatography (chloroform) to obtain 1.11 g of the title compound as a colorless oil.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05475024 |
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| 出典データセット | uspto-grants-1995_12 |
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| ORD ID | ord-53646cb0981b4fea8f37799922f0d9e8 |
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| 出典メモ | uspto-grants-1995_12 |
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