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Dichloromethane → N-(tert-butyl)-N'-[2-hydroxy-1-(3-nitrophenyl)ethyl]thiourea
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Dichloromethane | HCID 6344 | — |
| 反応物 | tert-Butyl isothiocyanate | HCID 11544 | — |
| 反応物 | 2-Amino-2-(3-nitrophenyl)ethan-1-ol | HCID 15752299 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 生成物 | N-(tert-butyl)-N'-[2-hydroxy-1-(3-nitrophenyl)ethyl]thiourea | HCID 22747831 | — |
反応手順
The process is performed as in Example 2, starting with 5.1 g of 2-amino-2-(3-nitrophenyl)-1-ethanol in 170 cm3 of ethanol containing 85 cm3 of dichloromethane and 4.6 cm3 of tert-butyl isothiocyanate, at a temperature in the region of 20° C. for 3 days and then at a temperature in the region of 60° C. for 7 hours. After addition of a further 0.35 cm3 of tert-butyl isothiocyanate and 16 hours at a temperature in the region of 60° C., an identical work-up gives 5.7 g of N-(tert-butyl)-N′-[2-hydroxy-1-(3-nitrophenyl)ethyl]thiourea in the form of an ocher-colored solid melting at 162° C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US06699895B2 |
| 出典データセット | uspto-grants-2004_03 |
| ORD ID | ord-8aad5d416b254211b007e94300ebbd9a |
| 出典メモ | uspto-grants-2004_03 |