関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Chloroacetonitrile | HCID 7856 | — |
| 反応物 | Ethyl 3-butoxy-3-sulfanylidenepropanoate | HCID 21317911 | — |
| 反応物 | Potassium methoxide | HCID 23664618 | — |
| 溶媒 | Methanol | HCID 887 | — |
| 生成物 | 5-Butoxy-3-hydroxythiophene-2-carbonitrile | HCID 21317900 | 41.1% |
反応手順
205 g of O-n-butyl 2-ethoxycarbonylthioacetate were added at 30° C. to a solution of 70 g of potassium methylate in a liter of methanol and the mixture was stirred for 10 minutes at 30° C. 75.5 g of chloroacetonitrile were added all at once to the mixture which was stirred for an hour at 40° C. and then a solution of 70 g of potassium methylate in 300 ml of methanol. The mixture was stirred for 6 hours at room temperature and was evaporated to dryness. The residue was washed with ethyl acetate and ether and was dried. The residue was then dissolved in water and the aqueous solution was acidified with concentrated hydrochloric acid and was vacuum filtered. The recovered precipitate was washed with water, dried and chromatographed over silica gel. Elution with 6-4 cyclohexane-ethyl acetate yielded 81 g of 2-cyano-3-hydroxy-5-n-butoxy-thiophene melting at 107° C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US04128562 |
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| 出典データセット | uspto-grants-1978_12 |
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| ORD ID | ord-c1e45e078eb043519707870911ab0059 |
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| 出典メモ | uspto-grants-1978_12 |
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