1-아미노옥시-3-아미노프로판

1-아미노옥시-3-아미노프로판
1-아미노옥시-3-아미노프로판 구조식 이미지
카스 번호:
98532-00-4
한글명:
1-아미노옥시-3-아미노프로판
동의어(한글):
1-아미노옥시-3-아미노프로판
상품명:
1-aminooxy-3-aminopropane
동의어(영문):
1-aminooxy-3-aminopropane;O-(3-aminopropyl)hydroxylamine
CBNumber:
CB71325123
분자식:
C3H10N2O
포뮬러 무게:
0
MOL 파일:
98532-00-4.mol

1-아미노옥시-3-아미노프로판 속성

안전

1-아미노옥시-3-아미노프로판 C화학적 특성, 용도, 생산

제조 방법

Over a 1-hr period, the temperature of a stirred solution of 150 gm (0.56 mole) of γ-bromopropylphthalimide, 91.7 gm (0.56 mole) of N-hydroxyphthalimide, 121 gm (1.2 moles) of triethylamine, and 700 ml of dimethyl formamide (DMF) is raised gradually to 90°C. The reaction mixture is cooled to room temperature and poured into 2 liters of water. The precipitate is collected (176 gm, 89.3%; m.p. 177-179°C). Upon re-crystallization (two times from glacial acetic acid, 8ml/gm), the melting point is raised to 178-180°C.
To a solution of 35.0 gm (0.1 mole) of 3-N-phthalimidopropyloxy-N-phthalimide in 200 ml of DMF maintained at 70°C is added 20 gm (0.4 mole) of hydrazine hydrate. After allowing the solution to cool to room temperature over a 1-hr period, 300 ml of cold water is added and the pH of the solution is adjusted to pH 3 with hydrochloric acid. The precipi­tated phthalhydrazide is separated by filtration; the filtrate is evaporated between 40 and 50°C under reduced pressure. The residue is dissolved in 1 liter of methanol and the resulting solution is passed through a column containing 1 liter of IRA-400 ion-exchange resin (in OH" form, and previously treated with methanol). After the eluant is collected the column is rinsed with 1.5 liters of methanol. The eluant and methanol rinsings are combined and concentrated under reduced pressure to afford 3.0 gm (45%), b.p. 110-115°C/3 mm Hg. On redistillation 2 gm (30%) of purified product is isolated; b.p. 99°C/40 mm Hg; n25D 1.4615; d254 0.999.
Preparation of 1-aminooxy-3-aminopropane

1-아미노옥시-3-아미노프로판 준비 용품 및 원자재

원자재

준비 용품


1-아미노옥시-3-아미노프로판 공급 업체

글로벌( 2)공급 업체
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Aladdin Scientific
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