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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 252256생성일: 2026년 10월 24일

Diethyl Ether → 958651-12-2

https://huagongshe.com/ko/reaction/252256

반응식

참여 물질

역할이름HCID투입량
반응물Diethyl EtherHCID 3283—
반응물Sulfuryl chlorideHCID 24648—
반응물1-Bromo-3-cyclopropylbenzeneHCID 3282672—
반응물ButyllithiumHCID 178418339—
용매HexaneHCID 8058—
용매Ether tetrahydrofuranHCID 21868444—
생성물958651-12-2HCID 55279574—

반응 조건

온도-78 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07868030B2
출처 데이터셋uspto-grants-2011_01
ORD IDord-94a9bcc3299841feb1fdc0123fafc4a7
출처 메모uspto-grants-2011_01