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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 411973Generated: October 26, 2026

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

https://huagongshe.com/reaction/411973

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantBenzhydryl isothiocyanateHCID 520742—
ReactantN-methyl aminooxy acetic acid hydrochlorideHCID 85852466—
SolventDiethyl EtherHCID 3283—
SolventChloroformHCID 6212—
Product[[[[(Benzhydryl)amino]thioxomethyl]methylamino]oxy]acetic acidHCID 1204503293.7%

Reaction Steps

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).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06562814B2
Source datasetuspto-grants-2003_05
ORD IDord-50183eaf6cae4780bfbc10c19dadfbdb
Source noteuspto-grants-2003_05