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HRID 374669생성일: 2026년 10월 24일

2-(Chloromethyl)-2,3-dihydro-1,4-benzodioxin → 2-Aminomethyl-1,4-benzodioxane

https://huagongshe.com/ko/reaction/374669

반응식

참여 물질

역할이름HCID투입량
반응물2-(Chloromethyl)-2,3-dihydro-1,4-benzodioxinHCID 95320—
반응물Phthalimide potassium saltHCID 24194345—
용매DimethylformamideHCID 6228—
생성물2-Aminomethyl-1,4-benzodioxaneHCID 15053—

반응 단계

Commercial grade of 2-chloromethyl-1,4-benzodioxane (10.0 g, 54.7 mmol) and phthalimide potassium salt (12.0 g, 65.0 mmol) were added to N,N-dimethylformamide (350 ml) and subjected to reaction overnight under reflux; thereafter, N,N-dlmethylformamide was distilled off under vacuum. Water (250 ml) was added to the residue and the mixture was stirred well, with the floating solids being subsequently recovered by filtration. The solids were dried, then recrystallized from methanol/methylene chloride, thereby yielding (1,4-benzodioxan-2-ylmethyl)phthalimide as a colorless tabular crystal in an amount of 8.43 g. The thus obtained crystal was dissolved in ethanol (500 ml); to the solution, hydrazine hydrate (4.3 g) was added, followed by refluxing under heating for 3 h. The resulting solids were filtered off and ethanol was distilled off under vacuum, followed by addition of water (300 ml). Thereafter, an aqueous solution of 6N sodium hydroxide was added to adjust pH to 12 and the mixture was subjected to 3 cycles of extraction with methylene chloride. The methylene chloride layers were dried with anhydrous sodium sulfate, and concentrated under vacuum, thereby yielding a crude product of 2-aminomethyl-1,4-benzodioxane as a colorless oil (crude product, 4.3 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05480905
출처 데이터셋uspto-grants-1996_01
ORD IDord-4e049f7f95094f20b49b427909f24510
출처 메모uspto-grants-1996_01