تفاعل #74931

ord-c0f10a5bdaf64f10bbb8a1599ba45e72

معادلة التفاعل

S
hydrogen sulfide
S=P12SP3(=S)SP(=S)(S1)SP(=S)(S2)S3
phosphorus pentasulfide
S
hydrogen sulfide
[Na+].[OH-]
sodium hydroxide
Cc1ccc(C(=O)CC(C(=O)c2ccccc2)c2ccccc2)cc1
1,2-diphenyl-4-p-tolylbutane-1,4-dione
Cc1ccc(-c2cc(-c3ccccc3)c(-c3ccccc3)s2)cc1
2,3-diphenyl-5-p-tolylthiophene
المردود 107.4%

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىThe autoclave was sealed
  2. 2
    درجة الحرارةchilled in a Dry Ice-acetone bath
  3. 3
    درجة الحرارةThe autoclave was then heated at 160°-190° C. (920-1130 psig) for 225 minutes
  4. 4
    أخرىThe slurry thus formed
  5. 5
    ترشيحwas filtered
  6. 6
    أخرىThe residue was dried

الإجراء التجريبي

In a 1-liter stainless steel autoclave equipped with stirrer were placed 71 g (0.217 mole) of 1,2-diphenyl-4-p-tolylbutane-1,4-dione, 100 ml of xylene, and 45 g (0.101 mole) of phosphorus pentasulfide. The autoclave was sealed, chilled in a Dry Ice-acetone bath, and charged with 120 g (3.52 moles) of hydrogen sulfide. The autoclave was then heated at 160°-190° C. (920-1130 psig) for 225 minutes. The autoclave was cooled to room temperature and the hydrogen sulfide vented into an aqueous sodium hydroxide solution. The residue in the autoclave was stirred with 150 ml of absolute ethanol. The slurry thus formed was filtered. The residue was dried to give 35.4 g (50.0%) of crude 2,3-diphenyl-5-p-tolylthiophene, m.p. 110°-112° C. Recrystallization from 190 ml. of toluene and 625 ml. of ethanol gave 30.1 g (42.5%) of pure 2,3-diphenyl-5-p-tolylthiophene, m.p. 114°-116° C.

المصدر

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