تفاعل #74935

ord-c97a814917c94e0094771d1c78b58c6e

معادلة التفاعل

S
hydrogen sulfide
S=P12SP3(=S)SP(=S)(S1)SP(=S)(S2)S3
phosphorus pentasulfide
S
hydrogen sulfide
[Na+].[OH-]
sodium hydroxide
COc1cccc(CC(=O)CC(C(=O)c2ccccc2)c2ccccc2)c1
1,2-diphenyl-4-m-anisylbutane-1,4-dione
COc1cccc(Cc2cc(-c3ccccc3)c(-c3ccccc3)s2)c1
2,3-diphenyl-5-m-anisylthiophene
المردود 82.3%

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةThe mixture was then heated
  2. 2
    أخرىto destroy excess phosphorus sulfides
  3. 3
    غسيلWashing the product with another 330 ml of ethanol
  4. 4
    أخرىgave 32 g (62.3%) of crude product
  5. 5
    أخرىRecrystallization from 50 ml of toluene and 150 ml of ethanol

الإجراء التجريبي

In a 1-liter stainless steel autoclave equipped with stirrer were placed 51.6 g (0.150 mole) of 1,2-diphenyl-4-m-anisylbutane-1,4-dione, 100 ml of xylene and 30 g (0.0675 mole) of phosphorus pentasulfide. The autoclave was cooled in Dry Ice and charged with 130 g (3.81 moles) of hydrogen sulfide. The mixture was then heated and stirred 235 minutes at 154°-177° C. (1120-1320 psig). The vessel was cooled to room temperature. The hydrogen sulfide was vented into a sodium hydroxide solution. The residue was treated with 150 ml of absolute ethanol to destroy excess phosphorus sulfides. Washing the product with another 330 ml of ethanol gave 32 g (62.3%) of crude product. Recrystallization from 50 ml of toluene and 150 ml of ethanol gave 19.8 g (38.5%) of pure 2,3-diphenyl-5-m-anisylthiophene, m.p. 100°-102° C.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US04174405uspto-grants-1979_11