反応式
Cl[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][OH:8].[NH2:9][C@H:10]([C:22](O)=O)CC1C=C2C(C=CC=C2)=CC=1.[CH3:25][C:26](C)=O>>[CH2:25]([N:9]([CH2:10][CH3:22])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][OH:8])[CH3:26]参加物
4
実験手順
A mixture of 10 ml (75 mmol) of 6-chlorohexanol and 16.9 g (112 mmole) of Nal dissolved in 100 ml acetone was refluxed for 3.5 days. The reaction mixture was filtered and the filtrate was concentrated to an oil and dissolved in 100 ml of ether. The ether solution was filtered, concentrated to an oil, and dissolved in 30 ml of diethylamine. The solution was stirred for 4 hours and filtered. The filtrate was concentrated to an oil, taken up in acidified water (pH<2) and washed with ethylacetate. The acidic solution was then adjusted to pH 9.5 and extracted twice with ethyl acetate. The organic extract was dried over MgSO4 and concentrated under vacuum to yield 7.5 g of the title compound as an oily product.
後処理
- temperaturewas refluxed for 3.5 days
- filtrationThe reaction mixture was filtered
- concentrationthe filtrate was concentrated to an oil
- dissolutiondissolved in 100 ml of ether
- filtrationThe ether solution was filtered
- concentrationconcentrated to an oil
- dissolutiondissolved in 30 ml of diethylamine
- filtrationfiltered
- concentrationThe filtrate was concentrated to an oil
- washwashed with ethylacetate
- extractionextracted twice with ethyl acetate
- extractionThe organic extract
- dry with materialwas dried over MgSO4
- concentrationconcentrated under vacuum
出典と根拠
- ORDレコード
- ord-44010693a68e471092ce8b62c2c8f065
- 出典データセット
- uspto-grants-1984_04
- 特許番号
- US04443440
関連ノート
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