Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | Formaldehyde | HCID 712 | — |
| Edukt | Chlorodiphenylphosphine | HCID 66180 | — |
| Edukt | Sodium Bicarbonate | HCID 516892 | — |
| Produkt | (Diphenylphosphoryl)methanol | HCID 608528 | 89% |
Reaktionsschritte
Hydroxymethyl diphenylphosphine oxide was prepared according to Lawrence & Jackson [J. Chem. Soc., Perkin Trans. 2002, 1, 2260]. To a mixture of HCl (18.9 ml) and aqueous formaldehyde (18.9 ml, 37 wt %) was added diphenyl chlorophosphine (2.80 ml, 10.6 mmol). The reaction mixture was heated to 100° C. for 18 hours under a nitrogen atmosphere. The reaction was neutralized with aqueous NaHCO3, and the aqueous phase was extracted with CH2Cl2 (3×30 ml). The organic phase was dried with anhydrous Na2SO4. Hydroxymethyl diphenylphosphine oxide (2.907 grams, 89% yield) was obtained after evaporation of the solvent as a colorless oil.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08318960B2 |
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| Quelldatensatz | uspto-grants-2012_11 |
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| ORD ID | ord-1340b952200f473085230618bfccf1e2 |
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| Quellennotiz | uspto-grants-2012_11 |
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