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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 326596생성일: 2026년 10월 24일

2-Methoxypropene → 6-bromo-2,2-dimethyl-4-(1,3-dithian-2-yl)-2H-1,3-benzoxazine

https://huagongshe.com/ko/reaction/326596

반응식

참여 물질

역할이름HCID투입량
반응물2-MethoxypropeneHCID 8300—
반응물1,3-DithianeHCID 10451—
반응물5-Bromo-2-hydroxybenzonitrileHCID 2757014—
반응물6-bromo-2,2-dimethyl-4-(1,3-dithian-2-yl)-2H-1,3-benzoxazineHCID 19735097—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
용매HexaneHCID 8058—
생성물6-bromo-2,2-dimethyl-4-(1,3-dithian-2-yl)-2H-1,3-benzoxazineHCID 19735097—
생성물5-Bromo-2-(2-methoxy-2-methylethoxy)benzonitrileHCID 19735126—

반응 단계

A solution (13.8 ml) of 1.6M n-butyllithium in hexane was added dropwise to a solution of 1,3-dithian (1.5 g) in anhydrous tetrahydrofuran (35 ml) at -78° C. under an argon atmosphere over 10 minutes. After stirring for 30 minutes, a solution of 5-bromo-2-(2-methoxy-2-methylethoxy)benzonitrile, which was prepared from 4-bromo-2-cyanophenol (m.p. 148°-150° C., 2.48 g) and 2-methoxypropene (1.1 g) according to the same manner as described in Example 29, in anhydrous tetrahydrofuran (5 ml) was added to the mixture. The mixture was treated in the same manner as that in Example 29 to obtain 6-bromo-2,2-dimethyl-4-(1,3-dithian-2-yl)-2H-1,3-benzoxazine (0.90 g) (Compound 105).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05270308
출처 데이터셋uspto-grants-1993_12
ORD IDord-30d90ac680874be6916d41865b13c04c
출처 메모uspto-grants-1993_12