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HRID 1491920作成日:2026年10月24日

1,5-Diiodopentane → 3-(4-Bromobutyl)-1-thia-3-azaspiro[5.4]decan-4-one

https://huagongshe.com/ja/reaction/1491920

反応式

関与物質

役割名称HCID仕込み量
反応物1,5-DiiodopentaneHCID 12354—
反応物Lithium HexamethyldisilazideHCID 2733832—
反応物3-(4-Bromobutyl)-4-thiazolidinoneHCID 10847505—
溶媒TetrahydrofuranHCID 8028—
生成物3-(4-Bromobutyl)-1-thia-3-azaspiro[5.4]decan-4-oneHCID 2170660063.8%

反応条件

温度-65 °C

反応手順

To a solution of 3-(4-bromobutyl)-4-thiazolidinone (25 g) in THF (350 ml) cooled to -60° C. was added 1,5-diiodopentane (100 g), and the resultant slurry was cooled to -65° C. A solution of lithium bis(trimethylsilyl)amide (0.220 mole) in hexanes (220 ml) was added dropwise, during which the internal temperature was maintained at or below -55° C. The addition was complete within 30 minutes. The mixture was stirred for additional 15 minutes at the same temperature and thereafter warmed to 0° C. with the aid of an ice bath. The mixture was stirred for additional 20 minutes and thereafter quenched with 500 ml of 0.5N HCl solution. The resultant mixture was placed under vacuum to remove some of the THF and thereafter extracted with ether (350 ml, 2×250 ml). The combined extracts were washed successively with water (400 ml) and brine (400 ml), dried with Na2SO4 and concentrated to a liquid. The liquid was chromatographed (2 silica gel columns) using 20-60% ethyl acetate/hexane as an eluent to obtain about 20.5 g of solid product.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05371087
出典データセットuspto-grants-1994_12
ORD IDord-b92dcca8f9e945c4a71810b24bb0b797
出典メモuspto-grants-1994_12