Pyridine → 2,2'-Bis(chloromethyl)-1,1'-biphenyl

To a reaction system comprising a suspension of 2,2'-bis(hydroxymethyl)-1,1'-biphenyl (85.3 grams, 0.398 mole) in methylene chloride (500 mL) at 0° C. containing pyridine (2 mL) was added a solution of thionyl chloride (163 grams, 1.36 moles) in methylene chloride (100 mL) dropwise with stirring. The system was allowed to warm to room temperature overnight and then was stripped to a residue with a stream of nitrogen at room temperature. The residue was dissolved in toluene (100 mL), cooled to 0° C., and quenched by the addition of ice cold, saturated sodium chloride solution (100 mL). The layers were separated, the organic phase was washed with water at 0° C. (1×100 mL), the layers separated, and the organic phase dried with magnesium sulfate. The solvent was evaporated to give a thick oil which was then distilled at 125° C. to 127° C. (0.1 mm Hg) to give 91.9 grams of colorless oil which contained 71.3 g of product dichloride (71% of theoretical yield).

1. customwas stripped to a residue with a stream of nitrogen at room temperature
2. temperaturecooled to 0° C.
3. customquenched by the addition of ice cold, saturated sodium chloride solution (100 mL)
4. customThe layers were separated
5. washthe organic phase was washed with water at 0° C. (1×100 mL)
6. customthe layers separated
7. dry with materialthe organic phase dried with magnesium sulfate
8. customThe solvent was evaporated
9. customto give a thick oil which
10. distillationwas then distilled at 125° C. to 127° C. (0.1 mm Hg)

ORD-Eintrag

ord-51838ee16c3a4a8ba5ab685aaae8176a

Quelldatensatz

uspto-grants-1989_11

DOI

10.6084/m9.figshare.5104873.v1

Patentnummer

US04879416