関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Allyl isocyanate | HCID 15123 | — |
| 反応物 | 3-[4-(Trifluoromethyl)phenoxy]azetidine | HCID 12812499 | — |
| 溶媒 | Diisopropyl Ether | HCID 7914 | — |
| 生成物 | N-(2-Propenyl)-3-[4-(trifluoromethyl)phenoxy]-1-azetidinecarboxamide | HCID 15053419 | — |
反応手順
A solution of 8.7 g (0.04 mole) of crude 3-[4-(trifluoromethyl)phenoxy]azetidine in 75 ml of isopropyl ether was stirred under a blanket of nitrogen while 4.2 g (0.05 mole) of 2-propenyl isocyanate was added dropwise. After stirring for 3 days, no crystalline product precipitated. The reaction mixture was concentrated to a dark reddish oil. TLC (20% ethyl acetate/methylene chloride on silica gel) showed at least 6 spots, all well separated. The residue was dissolved in chloroform, chromatographed on a 350 g silica gel column and eluted with chloroform until the reddish forerun was removed. The column was then eluted with an ethyl acetate/chloroform gradient to 4% ethyl acetate. All the fractions were combined and concentrated to give 4.8 of orange oil, which crystallized on standing. Recrystallization from acetone/cyclohexane gave 3.3 g (27.5%) of being crystals, m.p. 91°-92.5° C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05068231 |
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| 出典データセット | uspto-grants-1991_11 |
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| ORD ID | ord-2d60b1d155fa44878f040481b455c353 |
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| 出典メモ | uspto-grants-1991_11 |
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