HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1487928Generated: October 30, 2026
Diphenylphosphinic chloride → O-(Diphenylphosphinyl)hydroxylamine
https://huagongshe.com/reaction/1487928
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diphenylphosphinic chloride | HCID 73910 | — |
| Reactant | Hydroxyamine hydrochloride | HCID 443297 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Solvent | 1,4-Dioxane--water (1/1) | HCID 21886435 | — |
| Product | O-(Diphenylphosphinyl)hydroxylamine | HCID 10955453 | 49.6% |
Reaction Steps
Into a 500-mL three neck round-bottom flask, was placed a solution of hydroxylamine hydrochloride (30.0 g, 432 mmol) in H2O/dioxane (90/45 mL). The solution was cooled to 0-5° C., then sodium bicarbonate (36.5 g, 434 mmol) was added portion-wise over 10 min and the mixture was stirred at 0-5° C. for 30 min. A solution of diphenylphosphinoyl chloride (41.0 g, 173 mmol) in dioxane (45 mL) was added drop-wise at 0-5° C. over 30 min, then the resulting mixture was stirred for an additional 2 h at ambient temperature. The resulting solids were collected by filtration and washed with water (200 mL), NaOH (0.25 M, 200 mL) and PE (200 mL). The product was dried to yield the title compound as a white solid (20 g, crude).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09428502B2 |
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| Source dataset | uspto-grants-2016_08 |
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| ORD ID | ord-812142c8ee7940e78e4f6d2daef391c2 |
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| Source note | uspto-grants-2016_08 |
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