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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 919360Generated: October 30, 2026

Methanol → N'-Hydroxybenzenecarboximidamide

https://huagongshe.com/reaction/919360

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantBenzonitrileHCID 7505—
ReactantSodium HydroxideHCID 14798—
ReactantHydroxyamine hydrochlorideHCID 443297—
ProductN'-HydroxybenzenecarboximidamideHCID 69186—

Reaction Conditions

Temperature57.5 °C

Reaction Steps

Hydroxylamine hydrochloride (8.85 g, 0.126 moles) and methanol (45 mL) were charged to a 100 mL flask, followed by 51% sodium hydroxide (9.82 g, 0.125 moles). To this mixture was added benzonitrile (10.32 g, 0.100 moles), and the reaction was heated to 55-60° C. and held for 2 hours. HPLC showed that the reaction was complete by the disappearance of benzonitrile. A portion of the methanol (30 mL) was removed by distillation, deionized (DI) water was added (22 mL), and the remaining methanol was distilled at 300 torr to give two liquid phases (benzamide oxime melt and salt water). 2-Methyltetrahydrofuran (20.0 g) was added, and the aqueous salt phase was drained off to give 33.34 g of a solution of benzamide oxime in 2-methyltetrahydrofuran, 39.45% by loss on drying and HPLC. The yield of benzamide oxime was 96.5%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09273037B2
Source datasetuspto-grants-2016_03
ORD IDord-2f5a279cc92d48e59a7a738a222edc01
Source noteuspto-grants-2016_03