戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 232435作成日:2026年10月26日

Hexane → (+)-Methyl 5-(3-(2-(7-chloroquinolin-2-yl)ethenyl)phenyl)-8-dimethylcarbamyl-4,6-dithiaoctanoate

https://huagongshe.com/reaction/232435

反応式

関与物質

役割名称HCID仕込み量
反応物HexaneHCID 8058—
反応物Ammonium AcetateHCID 517165—
反応物(+)-Methyl 5-(3-formylphenyl)-8-dimethylcarbamyl-4,6-dithiaoctanoateHCID 19930537—
反応物7-Chloroquinolin-2-yl-methyltriphenylphosphonium bromideHCID 86743270—
反応物ButyllithiumHCID 178418339—
溶媒TetrahydrofuranHCID 8028—
生成物(+)-Methyl 5-(3-(2-(7-chloroquinolin-2-yl)ethenyl)phenyl)-8-dimethylcarbamyl-4,6-dithiaoctanoateHCID 86743269—

反応条件

温度-78 °C

反応手順

To a suspension of 7-chloroquinolin-2-yl-methyltriphenylphosphonium bromide (Example 4, Step 2) (809 mg, 1.56 mmol.) in THF (15 mL) at -78° C., was added a soltuion of n-BuLi (1.6M) in hexane (0.89 mL, 1.43 mmol.). The mixture was stirred for 0.5 hrs at -78° C. Then, (+)-methyl 5-(3-formylphenyl)-8-dimethylcarbamyl-4,6-dithiaoctanoate (step 3) (480 mg, 1.3 mmol.) in THF (4 mL) was slowly added. The mixture was stirred for 0.5 hr at -78° C. and then warmed up to room temperature and stirred for an additional 2 hrs. A solution of 25% ammonium acetate was added, the mixture was extracted with ethyl acetate, and the extracts were washed with brine (3×), dried over sodium sulfate, filtered and evaporated to dryness. Purification by flash chromatography afforded the title compound.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04851409
出典データセットuspto-grants-1989_07
ORD IDord-fdd911163de74c1e8ce6564324682e6b
出典メモuspto-grants-1989_07