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  2. Phosphorus trichloride - Wikipedia

    en.wikipedia.org/wiki/Phosphorus_trichloride

    Phosphorus trichloride is commonly used to convert primary and secondary alcohols to the corresponding chlorides. [14] As discussed above, the reaction of alcohols with phosphorus trichloride is sensitive to conditions. The mechanism for the ROH →RCl conversion involves the reaction of HCl with phosphite esters: P(OR) 3 + HCl ⇌ HP(OR) + 3 ...

  3. Phosphorus trichloride (data page) - Wikipedia

    en.wikipedia.org/wiki/Phosphorus_trichloride...

    The handling of this chemical may incur notable safety precautions. It is highly recommend that you seek the Material Safety Datasheet for this chemical from a reliable source such as SIRI, and follow its directions.

  4. Thiophosphoryl chloride - Wikipedia

    en.wikipedia.org/wiki/Thiophosphoryl_chloride

    Thiophosphoryl chloride has tetrahedral molecular geometry and C 3v molecular symmetry, with the structure S=PCl 3.According to gas electron diffraction, the phosphorus–sulfur bond length is 189 pm and the phosphorus–chlorine bond length is 201 pm, while the Cl−P−Cl bond angle is 102°.

  5. Phosphoryl chloride - Wikipedia

    en.wikipedia.org/wiki/Phosphoryl_chloride

    Phosphoryl chloride (commonly called phosphorus oxychloride) is a colourless liquid with the formula P O Cl 3. It hydrolyses in moist air releasing phosphoric acid and fumes of hydrogen chloride. It is manufactured industrially on a large scale from phosphorus trichloride and oxygen or phosphorus pentoxide. [4] It is mainly used to make ...

  6. Phosphorus halide - Wikipedia

    en.wikipedia.org/wiki/Phosphorus_halide

    Phosphorus trichloride is a major industrial chemical and widely used starting material for phosphorus chemistry. Phosphorus tribromide is used in organic chemistry to convert alcohols to alkyl bromides and carboxylic acids to acyl bromides ( e.g. in the Hell-Volhard-Zelinsky reaction ).

  7. Phosphinous acids - Wikipedia

    en.wikipedia.org/wiki/Phosphinous_acids

    Phosphinous acids are usually organophosphorus compounds with the formula R 2 POH. They are pyramidal in structure. Phosphorus is in the oxidation state III. Most phosphinous acids rapidly convert to the corresponding phosphine oxide, which are tetrahedral and are assigned oxidation state V.

  8. Diethylphosphite - Wikipedia

    en.wikipedia.org/wiki/Diethylphosphite

    The compound was probably prepared in the 1850s by combining phosphorus trichloride and ethanol, but intentional preparations came later. It arises as follows: [2] PCl 3 + 3 C 2 H 5 OH → (C 2 H 5 O) 2 P(O)H + 2 HCl + C 2 H 5 Cl. Under similar conditions but in the presence of base, triethyl phosphite results: [3]

  9. Phosphorochloridite - Wikipedia

    en.wikipedia.org/wiki/Phosphorochloridite

    In chemistry, phosphorochloridites are a class of organophosphorus compound with the formula (RO) 2 PCl (R = organic substituent). They are pyramidal in shape, akin to regular phosphites (P(OR) 3 ). They are usually colorless and sensitive toward hydrolysis and, to some extent, oxidation to the corresponding phosphorochloridates ((RO) 2 P(O)Cl).