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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1278686생성일: 2026년 10월 25일

Tetrahydrofuran → 2H-3,1-Benzoxazin-2-one, 1,4-dihydro-4,4-dimethyl-8-methoxy-

https://huagongshe.com/reaction/1278686

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참여 물질

역할이름HCID투입량
반응물TetrahydrofuranHCID 8028—
반응물Ammonium ChlorideHCID 25517—
반응물1,1'-CarbonyldiimidazoleHCID 68263—
반응물2-Amino-3-methoxybenzoic acidHCID 255720—
반응물HCID 178477779HCID 178477779—
용매Ethyl AcetateHCID 8857—
생성물2H-3,1-Benzoxazin-2-one, 1,4-dihydro-4,4-dimethyl-8-methoxy-HCID 21061756%

반응 조건

온도50 °C

반응 단계

To a solution of 2-amino-3-methoxybenzoic acid (5 g, 30 mmol) in anhydrous THF (100 mL) was added at ambient temperature under a blanket of nitrogen methylmagnesium bromide (3.0 M in THF, 50 mL, 150 mmol). The reaction mixture was heated at 50° C. for 18 hours, cooled to rt, and treated with a saturated aqueous ammonium chloride solution (50 mL). Ethyl acetate (100 mL) was added and organic layer was separated, dried (MgSO4), and evaporated. The residue was dissolved in anhydrous THF (100 mL) and treated at ambient temperature under nitrogen with 1,1′-carbonyldiimidazole (5.4 g, 33 mmol). After 24 hours, the mixture was quenched with 1N aqueous hydrogen chloride solution (30 mL). Ethyl acetate (100 mL) was added, organic layer was separated, dried (MgSO4), and evaporated. The residue was purified by a silica gel column chromatography (hexane:ethyl acetate/3:1) to afford 8-methoxy-4,4-dimethyl-1,4-dihydro-2H-3,1-benzoxazin-2-one as white solid (3.5 g, 56%): MS (ESI) m/z 208 [M+H]+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06444668B1
출처 데이터셋uspto-grants-2002_09
ORD IDord-571bac03bced488689e7e621305a237d
출처 메모uspto-grants-2002_09