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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 493461생성일: 2026년 10월 26일

Silane, trimethyl((1-methylethenyl)oxy)- → (4R,5R)-2-allyl-2-isopropenyloxy-4,5-bis-(1-methoxy-1-methyl-ethyl)-[1,3,2]dioxasilolane

https://huagongshe.com/reaction/493461

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참여 물질

역할이름HCID투입량
반응물Silane, trimethyl((1-methylethenyl)oxy)-HCID 74599—
반응물HCID 57681726HCID 57681726—
반응물HCID 178418348HCID 178418348—
용매PentaneHCID 8003—
생성물(4R,5R)-2-allyl-2-isopropenyloxy-4,5-bis-(1-methoxy-1-methyl-ethyl)-[1,3,2]dioxasilolaneHCID 5768174843.2%

반응 조건

온도0 °C

반응 단계

To a cooled (0° C.) solution of MeLi (13.0 mL; 21 mmol; 1.6 M in Et2O) was added 2-(trimethylsilyloxy)propene (2.8 g; 21 mmol). The solution was stirred 30 minutes at 0° C., and then warmed to room temperature and was stirred for 1 hour. The mixture was recooled to 0° C., and (4R,5R)-2-allyl-2-chloro-4,5-bis-(1-methoxy-1-methyl-ethyl)-[1,3,2]dioxasilolane (6.6 g; 21 mmol) was added. The mixture was warmed to room temperature and stirred for 2 hours. The solution was diluted with pentane (20 mL), and the mixture was then filtered through a pad of celite. The filtrate was concentrated, and the residue was distilled under reduced pressure to give 3.0 g (43%) of (4R,5R)-2-allyl-2-isopropenyloxy-4,5-bis-(1-methoxy-1-methyl-ethyl)-[1,3,2]dioxasilolane as a clear, colorless liquid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07534905B2
출처 데이터셋uspto-grants-2009_05
ORD IDord-395477f10ae54dd890ad556b2871b438
출처 메모uspto-grants-2009_05