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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 436108생성일: 2026년 10월 26일

Iodine → 4,4-Dimethyl-1-iodo-trans-1-octen-3-ol

https://huagongshe.com/reaction/436108

반응식

참여 물질

역할이름HCID투입량
반응물IodineHCID 807—
반응물Sodium HydroxideHCID 14798—
반응물Sodium ThiosulfateHCID 24477—
반응물Ethanamine, N,N-diethyl-, N-oxideHCID 123168—
반응물Bis(1,2-dimethylpropyl)boraneHCID 192733—
반응물2-[(4,4-Dimethyloct-1-YN-3-YL)oxy]oxaneHCID 14516370—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
용매DiglymeHCID 8150—
생성물4,4-Dimethyl-1-iodo-trans-1-octen-3-olHCID 20465723—

반응 단계

To 233 ml. of a 0.43M solution of disiamylborane in diglyme cooled to 0° C. under an inert atmosphere is added 23.8 g. (0.100 mole) 4,4-dimethyl-3-tetrahydropyranyloxy-1-octyne (Example 995). The mixture is allowed to come to room temperature and is stirred at ambient temperature for 3 hours. The solution is cooled to 0° C. and 22.5 g. (0.30 mole) of triethylamine oxide is added portionwise such that the temperature is maintained at 0°-5° C. The mixture is stirred at 0° C. for 1 hour and is then poured into 150 ml. of 1 N sodium hydroxide followed immediately by a solution of 25.4 g. (0.100 mole) of iodine in 60 ml. of tetrahydrofuran. The mixture is stirred at ambient temperatures for 0.5 hour and poured into 500 ml. of water. The mixture is decolorized by addition of sodium thiosulfate solution and is extracted into ether. The organic phase is washed with water and the solvent is removed in vacuo. The residue is stirred at room temperature for 20 hours with 900 ml. 3:1:1 tetrahydrofuran-acetic acid-water. The solution is evaporated in vacuo and the residue is chromatographed on silica gel in benzene using 10-20% ethylacetate in benzene.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04007210
출처 데이터셋uspto-grants-1977_02
ORD IDord-a9562b68861d49efbae522135db3cf18
출처 메모uspto-grants-1977_02