반응 #74932

ord-3023d7c751fc477492f211786f8263c2

반응 방정식

S
hydrogen sulfide
S=P12SP3(=S)SP(=S)(S1)SP(=S)(S2)S3
phosphorus pentasulfide
S
hydrogen sulfide
[Na+].[OH-]
sodium hydroxide
O=C(CC(C(=O)c1ccccc1)c1ccccc1)c1ccc(Cl)cc1
1,2-diphenyl4-p-chlorophenylbutane-1,4-dione
Clc1ccc(-c2cc(-c3ccccc3)c(-c3ccccc3)s2)cc1
2,3-diphenyl-5-p-chlorophenylthiophene
수율 134.7%

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    온도The autoclave was cooled with a Dry Ice-acetone bath
  2. 2
    온도The autoclave was heated
  3. 3
    온도The autoclave was cooled
  4. 4
    여과Filtration
  5. 5
    기타drying
  6. 6
    기타gave a crude product of 61.2 g (80.2%) m.p. 115°-117°
  7. 7
    기타Recrystallization from 190 ml of toluene and 625 ml of ethanol

실험 절차

In a 1-liter stainless steel autoclave equipped with stirrer were placed 76.9 g (0.220 mole) of 1,2-diphenyl4-p-chlorophenylbutane-1,4-dione, 100 ml of xylene and 45 g (0.101 mole) of phosphorus pentasulfide. The autoclave was cooled with a Dry Ice-acetone bath and charged with 120 g (3.52 moles) of hydrogen sulfide. The autoclave was heated with stirring for 200 minutes at 155°-178° C. (1000-2000 psig). The autoclave was cooled and the hydrogen sulfide allowed to escape into a sodium hydroxide solution. The residue was stirred with 150 ml of absolute ethanol. Filtration and drying gave a crude product of 61.2 g (80.2%) m.p. 115°-117°. Recrystallization from 190 ml of toluene and 625 ml of ethanol gave 47.2 g (61.9%) of pure 2,3-diphenyl-5-p-chlorophenylthiophene, m.p. 121°-122° C.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US04174405uspto-grants-1979_11