참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | Benzhydryl isothiocyanate | HCID 520742 | — |
| 반응물 | N-methyl aminooxy acetic acid hydrochloride | HCID 85852466 | — |
| 용매 | Diethyl Ether | HCID 3283 | — |
| 용매 | Chloroform | HCID 6212 | — |
| 생성물 | [[[[(Benzhydryl)amino]thioxomethyl]methylamino]oxy]acetic acid | HCID 12045032 | 93.7% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06562814B2 |
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| 출처 데이터셋 | uspto-grants-2003_05 |
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| ORD ID | ord-50183eaf6cae4780bfbc10c19dadfbdb |
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| 출처 메모 | uspto-grants-2003_05 |
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