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HRID 411973作成日:2026年10月24日

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

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

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物Benzhydryl isothiocyanateHCID 520742—
反応物N-methyl aminooxy acetic acid hydrochlorideHCID 85852466—
溶媒Diethyl EtherHCID 3283—
溶媒ChloroformHCID 6212—
生成物[[[[(Benzhydryl)amino]thioxomethyl]methylamino]oxy]acetic acidHCID 1204503293.7%

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06562814B2
出典データセットuspto-grants-2003_05
ORD IDord-50183eaf6cae4780bfbc10c19dadfbdb
出典メモuspto-grants-2003_05