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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1416178생성일: 2026년 10월 27일

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

https://huagongshe.com/reaction/1416178

반응식

참여 물질

역할이름HCID투입량
반응물3-MethoxybenzenethiolHCID 84989—
반응물6-Bromo-2,2,3-trimethyl-2H-benzo[b]pyranHCID 14956089—
반응물Sodium t-butoxideHCID 23676156—
촉매Tetrakis(triphenylphosphine)palladiumHCID 11979704—
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(O) (0.35 g) were added and the mixture was heated under reflux under a nitrogen atmosphere for 48 hours. Further tetrakis(triphenylphosphine)palladium(O) (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 번호US05912244
출처 데이터셋uspto-grants-1999_06
ORD IDord-93d3b7e6ae6c47ad8c7c63f53a437795
출처 메모uspto-grants-1999_06