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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1246621생성일: 2026년 10월 23일

1,2-Dibromoethane → 2,3-Dihydro-1,4-benzoxathiin-6-ol

https://huagongshe.com/ko/reaction/1246621

반응식

참여 물질

역할이름HCID투입량
반응물1,2-DibromoethaneHCID 7839—
반응물Potassium CarbonateHCID 11430—
반응물2-Mercaptobenzene-1,4-diolHCID 2736167—
용매AcetoneHCID 180—
생성물2,3-Dihydro-1,4-benzoxathiin-6-olHCID 1251591055.2%

반응 단계

1,2-Dibromoethane (2.3 mL, 26.7 mmol) and K2CO3 (8.21 g, 59.4 mmol) were slurried in acetone (250 mL) and a solution of 2-sulfanyl-1,4-benzenediol (prepared according to J. Org. Chem. 1990, 55, 2736) (4.22 g, 29.7 mmol) in acetone (50 mL) was added over 4 h to the stirred mixture. Once the addition was complete stirring was continued for a further 10 h before the solvent was removed in vacuo. The residue was partitioned between water (50 mL) and EtOAc (50 mL), the aqueous layer was extracted with EtOAc (50 mL) and the combined organic layers were dried (MgSO4) and evaporated. Purification of the residue by column chromatography [SiO2; 9:1 (pentane/EtOAc)] gave the title compound (2.48 g, 55%) as a pale orange oil; δH (CDCl3, 400 MHz) 3.08 (2H, m), 4.31 (2H, m), 4.44 (1H, s), 6.42 (1H, d), 6.49 (1H, s), 6.66 (1H, d); MS m/z (ES−) 167 (M−H+).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07129234B2
출처 데이터셋uspto-grants-2006_10
ORD IDord-31422edad81740f2b974eb9bb032f709
출처 메모uspto-grants-2006_10