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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 354535생성일: 2026년 10월 24일

Methanol → (2,6-Dimethyl-3-nitrophenyl)methanol

https://huagongshe.com/ko/reaction/354535

반응식

참여 물질

역할이름HCID투입량
반응물MethanolHCID 887—
반응물2,6-Dimethylbenzoic acidHCID 12439—
반응물2,6-Dimethyl-3-nitrobenzoic acidHCID 239329—
용매TetrahydrofuranHCID 8028—
생성물2,6-Dimethyl-3-nitrobenzoic acidHCID 239329—
생성물(2,6-Dimethyl-3-nitrophenyl)methanolHCID 1048764188.3%

반응 단계

2,6-Dimethyl-3-nitrobenzoic acid was prepared by nitrating 2,6-dimethylbenzoic acid. A solution of 2,6-dimethyl-3-nitrobenzoic acid (30 grams, 0.15 mole) in tetrahydrofuran (100 ml) was stirred under nitrogen. Borane-methyl sulfide complex (20 ml, 0.2 mole) was added dropwise at room temperature. When one fourth of the borane complex had been added the reaction mixture was brought to reflux. Reflux continued for one hour after complete addition of the borane complex. The reaction mixture was cooled to 0°, and cold methanol (500 ml) was added dropwise until foaming ceased and then added rapidly. The solvent was evaporated, and the crude product was dissolved in methylene chloride and washed with 2 N sodium hydroxide. The solvent was removed by evaporation to give (2,6-dimethyl-3-nitrophenyl)methanol (12.0 grams; mp 84°-92°).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04375476
출처 데이터셋uspto-grants-1983_03
ORD IDord-de9954a06a1e436db4426b380dac932f
출처 메모uspto-grants-1983_03