HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 919363Generated: November 3, 2026
Methanol → N'-Hydroxybenzenecarboximidamide
https://huagongshe.com/reaction/919363
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 (88.5 g, 1.26 moles) and methanol (450 mL) were charged to a 1000 mL flask, followed by 51% sodium hydroxide (97.7 g, 1.25 moles). Benzonitrile (103.1 g, 1.00 moles) was added and the reaction was heated to 65-71° C. for 4 hours. HPLC showed that the reaction was complete by the disappearance of benzonitrile. A portion of the methanol (366 mL) was removed by distillation, DI water was added (200 mL), and the remaining methanol was distilled at 200 torr to give two liquid phases (benzamide oxime melt and salt water). Butyl acetate (650 mL) and DI water (100 mL) were added, and the aqueous salt phase was drained off. The butyl acetate solution was washed once with 100 mL of water to give 715.04 g of a blue-tinted cloudy solution of benzamide oxime in butyl acetate, 18.1% by loss on drying. Yield of benzamide oxime was 95.1% with a 3.4% yield of benzamide by-product.
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-ecae867646cb4e50baf8fc57aa4b3749 |
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| Source note | uspto-grants-2016_03 |
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