関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 1H-Indene, 2-methyl- | HCID 16587 | — |
| 反応物 | Ammonium Chloride | HCID 25517 | — |
| 反応物 | 4-(2-Chloroethyl)morpholine | HCID 76727 | — |
| 反応物 | Indene ether | HCID 86747629 | — |
| 反応物 | Butyllithium | HCID 178418339 | — |
| 溶媒 | Diethyl Ether | HCID 3283 | — |
| 溶媒 | Hexane | HCID 8058 | — |
| 生成物 | 2-methyl-3-(2-ethyl N-morpholinyl)indene | HCID 19095517 | 54% |
反応手順
16.4 g (0.126 mol) 2-methylindene was taken up in 150 ml dry ether under nitrogen atmosphere. A solution of 9.6 g (0.15 mol) n-butyl lithium (2.1 M) in hexane (62 ml) was added dropwise to the indene/ether solution. The resulting solution was stirred at room temperature for 2 hours and a solution of 3.5 g (0.18 mol) N-(2-chloroethyl)morpholine in 100 ml ether was added and stirred overnight. Saturated solution of ammonium chloride was added to the reaction mixture and the ether layer was extracted with 2N HCl. The acidic aqueous layer was then washed with ether twice and cooled in an ice bath, then neutralized with 35% sodium hydroxide and extracted with ether to give 16.3 g (54%) of the 2-methyl-3-(2-ethyl N-morpholinyl)indene (Formula II Rz=methyl; R3=R4=hydrogen; Alk=1,2-ethylene).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05292736 |
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| 出典データセット | uspto-grants-1994_03 |
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| ORD ID | ord-eb9d12dd997142e6a29dbf2c6d24972e |
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| 出典メモ | uspto-grants-1994_03 |
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