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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 391699생성일: 2026년 10월 24일

Sodium Azide → 1-Fluoro-2-isocyanato-4-methoxybenzene

https://huagongshe.com/ko/reaction/391699

반응식

참여 물질

역할이름HCID투입량
반응물Sodium AzideHCID 33557—
반응물Oxalyl chlorideHCID 65578—
반응물2-Fluoro-5-methoxybenzoic acidHCID 2774543—
반응물HCID 57474799HCID 57474799—
용매DimethylformamideHCID 6228—
용매DichloromethaneHCID 6344—
용매1,4-Dioxane--water (1/1)HCID 21886435—
생성물1-Fluoro-2-isocyanato-4-methoxybenzeneHCID 22150993—

반응 단계

(Z)-1-(2-Amino-1,2-dicyanovinyl)-3-(2-fluoro-5-methoxyphenyl)urea. 2-Fluoro-5-methoxybenzoic acid (0.62 g, 3.62 mmol) was dissolved in CH2Cl2 (15 mL) and DMF (0.5 mL). Oxalyl chloride (0.38 mL, 4.32 mmol) was added dropwise. The mixture was stirred for another 15 min. The reaction was concentrated and then taken up in dioxane (10 mL). Sodium azide (0.26 g, 3.96 mmol) in water/dioxane (1:1 v/v, 10 mL) was added to the acid chloride at 0° C. The mixture was stirred for 10 min. The reaction was partitioned between EtOAc and water. The layers were shaken and separated. The organic layer was dried over sodium sulfate, filtered, and concentrated. The crude acyl azide was filtered through a silica gel plug (90% Hexanes in EtOAc. The filtrate was concentrated. The purified acyl azide was dissolved in toluene and stirred at 100° C. for 1 h. The toluene solution was concentrated to afford 1-fluoro-2-isocyanato-4-methoxybenzene in quantitative yield. 1-Fluoro-2-isocyanato-4-methoxybenzene (0.6 g, 3.62 mmol) was reacted with 2,3-diaminomaleonitrile (0.39 g, 3.62 mmol) according to General Procedure A to afford the title compound. MS (ESI) m/z 276.4 [M+1]+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08383634B2
출처 데이터셋uspto-grants-2013_02
ORD IDord-81bf7fa3d1c3454da3e25ffe2c2865cc
출처 메모uspto-grants-2013_02