تفاعل #67886

ord-8bc20bd6395941389bf10f1441644e6e

معادلة التفاعل

Brc1cccc(-c2ccccc2)c1
3-bromobiphenyl
C1COCCO1
1,4-dioxane
COc1cccc(OC)c1-c1ccccc1P(C1CCCCC1)C1CCCCC1
2-dicyclohexylphosphino-2′,6′-dimethoxybiphenyl
NN.O
hydrazine hydrate
COc1cccc(OC)c1-c1ccccc1P(=O)(C1CCCCC1)C1CCCCC1
2′-(dicyclohexyl-phosphinoyl)-2,6-dimethoxy-biphenyl

ظروف التفاعل

درجة الحرارة
94°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.ADDITIONwere added
  2. 2
    أخرىthe obtained reaction mixture
  3. 3
    درجة الحرارةThe reaction mixture was cooled to room temperature
  4. 4
    درجة الحرارةby heating
  5. 5
    درجة الحرارةto reflux for 40 min
  6. 6
    درجة الحرارةThe reaction mixture was cooled to room temperature
  7. 7
    ترشيحfollowed by filtration with celite
  8. 8
    أخرىThe organic layer of the filtrate was separated
  9. 9
    غسيلwashed with saline
  10. 10
    أخرىThe solvents were evaporated under reduced pressure from the organic layer
  11. 11
    أخرىthe obtained residue was purified with NH-silica gel column chromatography (ethyl acetate)

الإجراء التجريبي

To the mixture of 3-bromobiphenyl (0.020 ml, 0.12 mmol) and 1,4-dioxane (1.5 ml), water (0.15 ml), potassium phosphate tribasic n-hydrate (170 mg, 0.72 mmol), sodium 1,3-dioxo-1,3-dihydro-isoindole-2-ylmethyl trifluoroborate (60 mg, 0.24 mmol), palladium(II) acetate (2.7 mg, 0.012 mmol), and 2-dicyclohexylphosphino-2′,6′-dimethoxybiphenyl (9.9 mg, 0.024 mmol) were added, and then the obtained reaction mixture was stirred at 94° C. (an outer temperature) overnight. The reaction mixture was cooled to room temperature, and then hydrazine hydrate (48 mg, 0.96 mmol) and methanol (2 ml) were added thereto, followed by heating to reflux for 40 min. The reaction mixture was cooled to room temperature, and then ethyl acetate and water were added to the reaction mixture, followed by filtration with celite. The organic layer of the filtrate was separated and washed with saline. The solvents were evaporated under reduced pressure from the organic layer, and then the obtained residue was purified with NH-silica gel column chromatography (ethyl acetate), thereby obtaining the entitled compound (11 mg, 51%) as the mixture with 2′-(dicyclohexyl-phosphinoyl)-2,6-dimethoxy-biphenyl (6.2 mg).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08524946B2uspto-grants-2013_09