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HRID 252256作成日:2026年10月26日

Diethyl Ether → 958651-12-2

https://huagongshe.com/reaction/252256

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Sulfuryl chlorideHCID 24648—
反応物1-Bromo-3-cyclopropylbenzeneHCID 3282672—
反応物ButyllithiumHCID 178418339—
溶媒HexaneHCID 8058—
溶媒Ether tetrahydrofuranHCID 21868444—
生成物958651-12-2HCID 55279574—

反応条件

温度-78 °C

反応手順

Bromo-3-cyclopropyl-benzene (1.0 g, 5.1 mmol) [prep.: J. Org. Chem. vol. 41, 2262-6 (1976)] was dissolved in dry THF/diethyl ether (1:1, 30 ml) under an argon atmosphere and cooled to −78° C. BuLi (1.6 M in hexanes, 3.2 ml, 5.1 mmol) was added dropwise and the reaction mixture was further stirred at low temperature for 15 min. This reaction mixture was added via cannula to a SO2 gas saturated solution of diethyl ether (20 ml) precooled to −78° C. The reaction mixture was stirred overnight at room temperature and concentrated under reduced pressure. The crude intermediate was suspended in n-hexane (4A sieves dried, 20 ml) and chilled (ice-water). A solution of sulfuryl chloride (0.3 ml, 3.6 mmol) in dry hexane (8 ml) was added dropwise to the stirred suspension and then the cold bath was removed. After 90 min at room temperature the reaction mixture was filtered (Speedex pad) and the filtrate was concentrated under reduced pressure to yield a yellow oil: 0.6 g, (67%) GC-MS: M=216.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07868030B2
出典データセットuspto-grants-2011_01
ORD IDord-94a9bcc3299841feb1fdc0123fafc4a7
出典メモuspto-grants-2011_01