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HRID 127526作成日:2026年10月26日

Methyl iodide → 4-(1-Hydroxyethyl)-2,3,4,9-tetrahydrothiopyrano[2,3-b]indole

https://huagongshe.com/reaction/127526

反応式

関与物質

役割名称HCID仕込み量
反応物Methyl iodideHCID 6328—
反応物Ammonium ChlorideHCID 25517—
反応物MagnesiumHCID 5462224—
反応物4-Formyl-2,3,4,9-tetrahydrothiopyrano[2,3-b]indoleHCID 14735629—
反応物HCID 178418373HCID 178418373—
溶媒BenzeneHCID 241—
溶媒Diethyl EtherHCID 3283—
生成物4-(1-Hydroxyethyl)-2,3,4,9-tetrahydrothiopyrano[2,3-b]indoleHCID 20284777—

反応手順

Methyl magnesium iodide prepared from reaction of magnesium (2.4 g) and methyl iodide (13.9 g) in absolute ether is dissolved in absolute benzene (50 ml) and a solution of 4-formyl-2,3,4,9-tetrahydrothiopyrano[2,3-b]indole (5.5 g) in absolute benzene (60 ml) is added dropwise thereto during 3 hours. The mixture is stirred at room temperature for 1 hour, poured slowly into an ice water containing ammonium chloride (10 g) and extracted with ether. The extract is evaporated. The oily residue is chromatographed on a column of silica gel and eluted with ether-benzene (1:50). The eluate is evaporated. The residue is again chromatographed on a column of silica gel and eluted with benzene and ether-benzene (1:20). The title compound is obtained from the latter eluate as an oil (4.58 g).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04256640
出典データセットuspto-grants-1981_03
ORD IDord-c88c20fec02f4ae395639a69a822b0fe
出典メモuspto-grants-1981_03