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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 411973생성일: 2026년 10월 24일

Triethylamine → [[[[(Benzhydryl)amino]thioxomethyl]methylamino]oxy]acetic acid

https://huagongshe.com/ko/reaction/411973

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Benzhydryl isothiocyanateHCID 520742—
반응물N-methyl aminooxy acetic acid hydrochlorideHCID 85852466—
용매Diethyl EtherHCID 3283—
용매ChloroformHCID 6212—
생성물[[[[(Benzhydryl)amino]thioxomethyl]methylamino]oxy]acetic acidHCID 1204503293.7%

반응 단계

A mixture of benzhydryl-isothiocyanate (13.75 g), N-methyl aminooxy acetic acid hydrochloride (8.6 g), triethylamine (16 g) and chloroform (200 mL) was heated at reflux for three hours, stirred at ambient temperature for one hour. The mixture was diluted with chloroform (200 mL) and washed with 2N HCl (2×300 mL) then with water (300 mL). The organic phase was dried over anhydrous magnesium sulfate and evaporated to dryness to give a solid. The solid was stirred in ether (200 mL) and filtered to give 18.8 g of [[[[(benzhydryl)amino]thioxomethyl]methylamino]oxy]acetic acid as a white solid, m.p. 160-162° C. Mass spectrum (−FAB, [M−H]−) m/z 329. 1H-NMR (DMSO-d6; 400 MHz) δ13.55 (br s, 1H), 9.75 (d, 1H), 7.35-7.23 (m, 10H), 6.63 (d, 1H), 4.63 (s, 2H), and 3.42 ppm (s, 3H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06562814B2
출처 데이터셋uspto-grants-2003_05
ORD IDord-50183eaf6cae4780bfbc10c19dadfbdb
출처 메모uspto-grants-2003_05