反応式
[NH2:1][CH2:2][CH2:3][OH:4].[C:5](OCC)(=[O:12])[C:6]1[CH:11]=[CH:10][CH:9]=[N:8][CH:7]=1>>[OH:4][CH2:3][CH2:2][NH:1][C:5]([C:6]1[CH:7]=[N:8][CH:9]=[CH:10][CH:11]=1)=[O:12]参加物
3
実験手順
A neat mixture of 2-aminoethanol (6.1 g, 0.10 mol) and ethyl nicotinate (15.1 g, 0.10 mol) was refluxed overnight. As the mixture was cooled to room temperature, the product precipitated as a crystalline solid. It was filtered, washed with ether and then recrystallized from 2-propanol/ether. The final product was collected by vacuum filtration and washed with ether. The dried, white compound weighed 10.7 g, resulting in a 64.5% yield; mp 88.5°-89.5° C. (lit. value 92° C.).
後処理
- temperaturewas refluxed overnight
- customthe product precipitated as a crystalline solid
- filtrationIt was filtered
- washwashed with ether
- customrecrystallized from 2-propanol/ether
- filtrationThe final product was collected by vacuum filtration
- washwashed with ether
- customresulting in a 64.5% yield
- custommp 88.5°-89.5° C. (lit. value 92° C.)
出典と根拠
- ORDレコード
- ord-3712d954fac542b6ac570c680ac34ead
- 出典データセット
- uspto-grants-1991_03
- 特許番号
- US05002935
関連ノート
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