関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Water | HCID 962 | — |
| 反応物 | Sodium | HCID 5360545 | — |
| 反応物 | O-(p-toluenesulfonyl)-m-phenoxymandelonitrile | HCID 12945136 | — |
| 反応物 | HCID 178418395 | HCID 178418395 | — |
| 溶媒 | 1,2-Dimethoxyethane | HCID 8071 | — |
| 生成物 | alpha-(2-Benzothiazolylthio)(m-phenoxyphenyl)acetonitrile | HCID 20532030 | 85% |
反応手順
1.517 g of O-[p-toluenesulfonyl)-m-phenoxymandelonitrile was dissolved in 5 ml of DME, and the solution was stirred in an argon atmosphere under ice cooling. Sodium salt of 2-mercaptobenzothiazole (760 mg) was added, and the mixture was stirred under ice cooling for 30 minutes, and then at room temperature for 1.5 hours. Water (20 ml) was added to the reaction mixture, and it was extracted with 20 ml of methylene chloride three times. The extract was washed with 10 ml of water, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was purified by column chromatography (silica gel; benzene and methylene chloride) to afford 1.233 g (yield 85%) of alpha-(2-benzothiazolylthio)(m-phenoxyphenyl)acetonitrile 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 | US04340740 |
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| 出典データセット | uspto-grants-1982_07 |
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| ORD ID | ord-9978d8620b444b699ef6db7c7ebd0a78 |
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| 出典メモ | uspto-grants-1982_07 |
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