돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 414129생성일: 2026년 10월 24일

Iodine → 3(2-Propynyl)benzaldehyde ethylene acetal

https://huagongshe.com/ko/reaction/414129

반응식

참여 물질

역할이름HCID투입량
반응물IodineHCID 807—
반응물Ammonium ChlorideHCID 25517—
반응물2-(3-Bromophenyl)-1,3-dioxolaneHCID 87306—
반응물1-Methoxypropa-1,2-dieneHCID 139403—
촉매Cuprous chlorideHCID 62652—
용매TetrahydrofuranHCID 8028—
생성물3(2-Propynyl)benzaldehyde ethylene acetalHCID 21282857—

반응 단계

Dry Mg (0.74 g) under dry N2 in a flask is covered with THF (10 ml) and a crystal I2 added. 5 ml of a solution of 3-bromobenzaldehyde ethylene acetal (7.0 g) in THF (30 ml) is added and kept until it becomes warm, when it is cooled to 15°, and the remainder of the acetal solution added over 15 minutes, then stirred for an additional 1 hour. A mixture of methoxyallene (2.45 g), copper (1)chloride (0.30 g) and THF (30 ml) is cooled to -20°. The above Grignard solution (under moisture excluding conditions) is then added to this solution during 5 minutes, and allowed to warm to 20° with stirring over 30 minutes. Saturated aqueous ammonium chloride is added and the product is extracted with ether. The ether layer is washed with water, dried (MgSO4) and the residue distilled in vacuo. Yield 4.3 g (75%) 89°-96° (0.03 m Hg), nD20 1.5422.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04789754
출처 데이터셋uspto-grants-1988_12
ORD IDord-e211f82262d5466591bb47f9cc3c9d80
출처 메모uspto-grants-1988_12