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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 851286생성일: 2026년 10월 26일

Methanol → 2-Bromo-4-(dimethoxymethyl)-1-fluorobenzene

https://huagongshe.com/reaction/851286

반응식

참여 물질

역할이름HCID투입량
반응물MethanolHCID 887—
반응물Trimethyl orthoformateHCID 9005—
반응물3-Bromo-4-fluorobenzonitrileHCID 123579—
촉매NickelHCID 935—
용매Formic AcidHCID 284—
용매WaterHCID 962—
생성물2-Bromo-4-(dimethoxymethyl)-1-fluorobenzeneHCID 2226086475%

반응 단계

A mixture of 85 g of Raney nickel, which had been washed thoroughly with water, 500 ml of formic acid and 100 g (0.5 mole) of 3-bromo-4-fluoro-benzonitrile was stirred for 24 hours at 90°-100° C. under an atmosphere of a blanketing gas (nitrogen or argon). After cooling to room temperature, 1 liter of water was added and the mixture was extracted twice with 300 ml of toluene. The combined toluene solutions were washed with 200 ml of water, with 200 ml of saturated sodium bicarbonate solution and again with 200 ml of water and then dried by incipient distillation. 1.5 g of air-dried ion exchanger SPC 118, 16 g (0.5 mole) of methanol and 58.5 g (0.55 mole) of orthoformic acid trimethyl ester were then added to the solution, the mixture was stirred for a further 1 hour without a bath and was then warmed at 50° C. for 2 hours. The reaction mixture was cooled, filtered to remove the ion exchanger and washed with 200 ml of 5% strength potassium carbonate solution. The solvent was then stripped off and the residue was distilled in vacuo. 93 g (75% of theory) of 3-bromo-4-fluoro-benzaldehyde dimethyl acetal were obtained in this way, in the form of a colorless liquid with a boiling point of 67°-68° C./0.1 mm Hg.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04383949
출처 데이터셋uspto-grants-1983_05
ORD IDord-04dc028d0ccc418897fc25f96e9ef5a1
출처 메모uspto-grants-1983_05