HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 919360Generated: October 30, 2026
Methanol → N'-Hydroxybenzenecarboximidamide
https://huagongshe.com/reaction/919360
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Benzonitrile | HCID 7505 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Hydroxyamine hydrochloride | HCID 443297 | — |
| Product | N'-Hydroxybenzenecarboximidamide | HCID 69186 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09273037B2 |
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| Source dataset | uspto-grants-2016_03 |
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| ORD ID | ord-2f5a279cc92d48e59a7a738a222edc01 |
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| Source note | uspto-grants-2016_03 |
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