関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 4-Nitrobenzaldehyde | HCID 541 | — |
| 反応物 | Diethyl chlorophosphate | HCID 13139 | — |
| 反応物 | p-Tolyl methyl sulfone | HCID 18521 | — |
| 反応物 | Butyllithium | HCID 178418339 | — |
| 溶媒 | Water | HCID 962 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 溶媒 | Hexane | HCID 8058 | — |
| 生成物 | 1-methyl-4-[(1E)-2-(4-nitrophenyl)ethenesulfonyl]benzene | HCID 13873807 | 98.1% |
反応手順
To 15 g (85.47 mmol) of methyl p-tolyl sulfone dissolved in 450 cm3 of tetrahydrofuran are added, at a temperature in the region of 0° C. under an argon atmosphere, 117.5 cm3 (188 mmol) of a 1.06 M solution of n-butyl-lithium in hexane. After stirring for 30 minutes at a temperature in the region of 0° C. are added, under an argon atmosphere, 13 cm3 (85.47 mmol) of diethylchlorophosphate dissolved in 70 cm3 of tetrahydrofuran. After stirring for 30 minutes at a temperature in the region of 0° C., the reaction mixture is cooled to a temperature in the region of −78° C., followed by addition, under an argon atmosphere, of 13.05 g (85.47 mmol) of 4-nitrobenzaldehyde dissolved in 130 cm3 of tetrahydrofuran. After stirring for 1 hour at a temperature in the region of −78° C., the temperature of the reaction mixture is allowed to rise to a temperature in the region of 20° C., 100 cm3 of water are added and the mixture is concentrated under reduced pressure (2.7 kPa) to give a beige-coloured solid. The solid is stirred in 250 cm3 of water for 20 minutes, filtered, washed with three times 40 cm3 of water and oven-dried under reduced pressure (2.7 kPa) at 35° C. for 5 hours to give 25.43 g of 1-[(E)-2-(4-methylphenyl)sulfonylvinyl]-4-nitrobenzene in the form of a beige-coloured solid melting at 176° C.; M.W.=303, IE: m/z=303 M+, m/z=239 [M-SO2]+, m/z=139 [CH3-Ph-SO]+.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07560571B2 |
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| 出典データセット | uspto-grants-2009_07 |
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| ORD ID | ord-ac38b2dc724141898525460096fd685f |
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| 出典メモ | uspto-grants-2009_07 |
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