反応式
C(OC([NH:8][C@@H:9]([CH3:15])[CH2:10][O:11][N+:12]([O-:14])=[O:13])=O)(C)(C)C.CCOCC.[ClH:21].O1CCOCC1>>[ClH:21].[CH3:15][C@H:9]([NH2:8])[CH2:10][O:11][N+:12]([O-:14])=[O:13]参加物
4
実験手順
In 80 ml of 4N hydrochloric acid-dioxane were dissolved 4.52 g of (1S)-N-(t-butoxycarbonyl)-1-methyl-2-nitroxyethylamine, and the mixture was left to stand at room temperature for 1 hour and 50 minutes. To the mixture were added 160 ml of ether, and the crystals were collected by filtration and dried to obtain 3.02 g of the desired compound as colorless crystals.
後処理
- waitthe mixture was left
- filtrationthe crystals were collected by filtration
- customdried
出典と根拠
- ORDレコード
- ord-21634171d01d4347a88d48f984cf1d4f
- 出典データセット
- uspto-grants-1999_04
- 特許番号
- US05891898
関連ノート
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