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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 422130생성일: 2026년 10월 25일

Diethyl Ether → ((1S,2R,4aS,8aS)-2-hydroxy-2,5,5,8a-tetramethyldecahydronaphthalen-1-yl)methyl methanesulfonate

https://huagongshe.com/reaction/422130

반응식

참여 물질

역할이름HCID투입량
반응물Diethyl EtherHCID 3283—
반응물TriethylamineHCID 8471—
반응물Methanesulfonyl chlorideHCID 31297—
반응물(1S,2R,4aS,8aS)-1-(hydroxymethyl)-2,5,5,8a-tetramethyl-decahydronaphthalen-2-olHCID 10879261—
용매DimethylformamideHCID 6228—
생성물((1S,2R,4aS,8aS)-2-hydroxy-2,5,5,8a-tetramethyldecahydronaphthalen-1-yl)methyl methanesulfonateHCID 5829478696%

반응 단계

To a mixture of (1S,2R,4aS,8aS)-1-(hydroxymethyl)-2,5,5,8a-tetramethyl-decahydronaphthalen-2-ol (3) (4.66 g, 19.4 mmol)) and Et3N (7.01 mL, 50.4 mmol)) in DMF (40 mL) was added methanesulfonyl chloride (2.66 g, 23.3 mmol) dropwise at 0° C. After stirring at room temperature for 3 h, ether (400 mL) was added. The organics were washed with 1N HCl (20 mL), saturated aqueous sodium bicarbonate (20 mL), brine (2×20 mL), dried (Na2SO4), and concentrated to give ((1S,2R,4aS,8aS)-2-hydroxy-2,5,5,8a-tetramethyldecahydronaphthalen-1-yl)methyl methanesulfonate (12) (5.90 g, 96%) as a light yellow sticky mass.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08101605B2
출처 데이터셋uspto-grants-2012_01
ORD IDord-c6e33cfc2154442db5fb475b53fc6eb5
출처 메모uspto-grants-2012_01