関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Water | HCID 962 | — |
| 反応物 | Carbofuran | HCID 2566 | — |
| 反応物 | Triethylamine | HCID 8471 | — |
| 反応物 | Amidosulfenyl chloride, N,N-dibutyl- | HCID 81031 | — |
| 触媒 | Triethylamine sulfur dioxide | HCID 12824984 | — |
| 溶媒 | Hexane | HCID 8058 | — |
| 生成物 | 2,3-Dihydro-2,2-dimethyl-7-benzofuranyl (dibutylaminothio)methylcarbamate | HCID 13206391 | 90% |
反応手順
A flask was charged with 30.2 g of a 50% solution of dibutylaminosulfenyl chloride (0.077 mole) in hexane and 15.8 g of 98% 2,3-dihydro-2,2-dimethyl-7-benzofuranyl methylcarbamate (0.07 mole) was added. Triethylamine (7.8 g, 0.077 mole) was added to the mixture with agitation over a period of seven minutes. A temperature rise from 24.5° to 26° C. was observed. A portion (1.9 g, 0.0115 mole) of the triethylamine/sulfur dioxide catalyst prepared in Example 3 was added dropwise. The temperature gradually rose to 30° C., and was raised further by external heating to 35° C. for a total reaction time of 100 minutes from the beginning of triethylamine addition. Twenty minutes later the mixture was cooled to 11° C. and 31 ml of water was added and mixed. The mixture was filtered to remove a small amount of solid, separated, and the organic layer was concentrated to yield 26.64 g of 90% (hplc) 2,3-dihydro-2,2-dimethyl-7-benzofuranyl (dibutylaminothio)methylcarbamate (a 90% chemical yield based on the starting carbamate).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US04329293 |
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| 出典データセット | uspto-grants-1982_05 |
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| ORD ID | ord-07ad1bb7582f4de9bbc9893b077fb3b8 |
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| 出典メモ | uspto-grants-1982_05 |
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