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HRID 2106844作成日:2026年10月25日

Diethyl Ether → (3S,4S,6R)-tetrahydro-3-hexyl-4-[(t-butyldimethylsilyl)oxy-]6-undecyl-2H-pyran-2-one

https://huagongshe.com/reaction/2106844

反応式

関与物質

役割名称HCID仕込み量
反応物Diethyl EtherHCID 3283—
反応物tert-Butyldimethylsilyl chlorideHCID 28928—
反応物(3S,4S,6R)-3-Hexyltetrahydro-4-hydroxy-6-undecyl-2H-pyran-2-oneHCID 11013671—
溶媒DimethylformamideHCID 6228—
生成物(3S,4S,6R)-tetrahydro-3-hexyl-4-[(t-butyldimethylsilyl)oxy-]6-undecyl-2H-pyran-2-oneHCID 2284745163.5%

反応手順

(M)(d) 1.5 g of (3S,4S,6R)-tetrahydro-3-hexyl-4-hydroxy-6-undecyl-2H-pyran-2-one were dissolved in 8 ml of DMF. 0.85 g of t-butyldimethylchlorosilane in 4 ml of DMF were then added dropwise. The mixture was stirred for 48 hours. The reaction mixture was poured in to 100 ml of ether and washed with 1N hydrochloric acid. The organic phase was dried, filtered and evaporated. The material obtained was chromatographed on silica gel. There were obtained 1.26 g of (3S,4S,6R)-tetrahydro-3-hexyl-4-[(t-butyldimethylsilyl)oxy]-6-undecyl-2H-pyran-2-one, MS: 411 (M+ -t-butyl).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04931463
出典データセットuspto-grants-1990_06
ORD IDord-443b7f69606d48689841134a0849a597
出典メモuspto-grants-1990_06