돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 845생성일: 2026년 10월 23일

Dimethyl Sulfoxide → 2-Fluoro-6-[(3-methyl-5-methoxyphenyl)thio]benzonitrile

https://huagongshe.com/ko/reaction/845

반응식

참여 물질

역할이름HCID투입량
반응물Dimethyl SulfoxideHCID 679—
반응물2,6-DifluorobenzonitrileHCID 74695—
반응물SulfurHCID 5362487—
반응물1-Bromo-3-methoxy-5-methylbenzeneHCID 10679554—
반응물CID 53628100HCID 178418400—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
용매Acetone cardiceHCID 18522661—
생성물2-Fluoro-6-[(3-methyl-5-methoxyphenyl)thio]benzonitrileHCID 10516388—

반응 단계

A solution of 1 g (0.005 mol) of 3-bromo-5-methoxytoluene in 10 mL of freshly distilled THF was cooled in dry ice/acetone and stirred under a N2 atmosphere. To this was added dropwise via a syringe 8.46 mL (0.011 mol) of sec-BuLi (1.3M in cyclohexane). The resultant mixture was stirred for 10 min after which 0.19 g of elemental sulfur was added in one portion. The reaction mixture was brought to room temperature and left stirring for 12 h. The mixture was cooled in ice/water bath. 0.69 g (0.005 mol) of 2,6-difluorobenzonitrile in 5 mL of dry DMSO was added. After sitting for 20 min, the mixture was poured into water (100 mL) and extracted with 3×50 mL of EtOAc. The EtOAc solution was washed with 1N NaOH, water, and dried over MgSO4Removal of EtOAc under vacuo resulted in a crude product which was chromatographed on silica gel (flash; EtOAc/Hexane 1:9). This resulted in 0.63 g (46%) of 2-fluoro-6-[(3-methyl-5-methoxyphenyl)thio]benzonitrile: mp 94°-95° C.; NMR (Me2SO-d6, 200 MHz) δ 2.28 (s, 3H), 3.7 (s, 3H), 6.8-7 (m, 4H), 7.34 (apparent d, 1H), 7.62 (dd, 1H). Anal. Calc. for C15H12NOSF: C, 65.92; H, 4.43; N, 5.12; S, 11.73. Found: C, 66.03; H, 4.49; N, 5.09; S, 11.8.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05723452
출처 데이터셋uspto-grants-1998_03
ORD IDord-6c9f5721435e410ba7c84870a32cbc44
출처 메모uspto-grants-1998_03