تفاعل #1509639

ord-55ba6f68ffa44527bcc5ebc89d24a7e2

معادلة التفاعل

CC(C)(C)P(C(C)(C)C)C(C)(C)C
tri-tert-butyl phosphine
Cc1ccc(Nc2ccc(C)cc2)cc1
Di-p-tolylamine
Brc1ccc(-c2ccc(Br)cc2)cc1
4,4′-dibromobiphenyl
CC(C)(C)[O-].[Na+]
Sodium tert-butoxide
Cc1ccc(N(c2ccc(C)cc2)c2ccc(-c3ccc(Br)cc3)cc2)cc1
material
المردود 3.0%
Cc1ccc(N(c2ccc(C)cc2)c2ccc(-c3ccc(Br)cc3)cc2)cc1
4′-bromo-N,N-di-p-tolylbiphenyl-4-amine
المردود 3.0%

ظروف التفاعل

درجة الحرارة
120°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىwas degassed in toluene (anhydrous, 50 mL) for 20 minutes
  2. 2
    أخرىthe mixture was further degassed for 15 minutes
  3. 3
    أخرىmixture was further degassed for 10 minutes
  4. 4
    درجة الحرارةAfter cooling
  5. 5
    workup.ADDITIONthe mixture was poured into DCM, and solids
  6. 6
    ترشيحwere filtered off
  7. 7
    غسيلFiltrate was washed with water and brine
  8. 8
    أخرىThe organic layer was collected
  9. 9
    تجفيفdried over sodium sulfate

الإجراء التجريبي

A mixture of tris(dibenzylideneacetone)dipalladium (353 mg, 0.385 mmol), and tri-tert-butyl phosphine (3.11 g of a 10% solution in hexanes) was degassed in toluene (anhydrous, 50 mL) for 20 minutes. Di-p-tolylamine (3.00 g, 15.2 mmol), and 4,4′-dibromobiphenyl (4.80 g, 15.4 mmol) were added and the mixture was further degassed for 15 minutes. Sodium tert-butoxide (2.4 g, 25 mmol) was added, and mixture was further degassed for 10 minutes. The whole was heated overnight at 120° C. under argon. After cooling, the mixture was poured into DCM, and solids were filtered off. Filtrate was washed with water and brine. The organic layer was collected and dried over sodium sulfate, then loaded onto silica gel. A flash column (gradient of 2-20% ethyl acetate in hexanes) gave 190 mg of material (3% yield); confirmed pure by HNMR.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08927121B2uspto-grants-2015_01