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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1420755생성일: 2026년 10월 27일

3-Methoxybenzenethiol → 6-(3-methoxyphenyl)thio-2,2,3-trimethyl-2H-benzo[b]pyran

https://huagongshe.com/reaction/1420755

반응식

참여 물질

역할이름HCID투입량
반응물3-MethoxybenzenethiolHCID 84989—
반응물6-Bromo-2,2,3-trimethyl-2H-benzo[b]pyranHCID 14956089—
반응물Sodium t-butoxideHCID 23676156—
촉매HCID 178418397HCID 178418397—
용매EthanolHCID 702—
생성물6-(3-methoxyphenyl)thio-2,2,3-trimethyl-2H-benzo[b]pyranHCID 1878287689.8%

반응 단계

6-Bromo-2,2,3-trimethyl-2H-benzo[b]pyran (6.5 g) (see Preparation 4) was dissolved in absolute ethanol (135 ml), then sodium tert-butoxide (7.5 g), 3-methoxybenzenethiol (3.6 g) and tetrakis(triphenylphosphine)palladium(0) (0.35 g) were added and the mixture was heated under reflux under a nitrogen atmosphere for 48 hours. Further tetrakis(triphenylphosphine)palladium(0) (0.3 g) was added and heating was continued for a further 48 hours. The solvent was removed under reduced pressure and the residue was dissolved in dichloromethane and washed with water. The organic layer was dried (anhydrous sodium sulphate), the solvent removed under reduced pressure and the crude product chromatographed on silica using 1:1 hexane:dichloromethane as the eluent to yield 6-(3-methoxyphenyl)thio-2,2,3-trimethyl-2H-benzo[b]pyran (7.2 g) as an oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06071938
출처 데이터셋uspto-grants-2000_06
ORD IDord-efbe90a7f78546fcac0fa747596e88cc
출처 메모uspto-grants-2000_06