تفاعل #985261

ord-5604215748e24f859d16b9a30f4d0eab

معادلة التفاعل

O=C(Cl)c1ccc([N+](=O)[O-])cc1
4-nitrobenzoyl chloride
Nc1ccccc1S
2-aminothiophenol
O=[N+]([O-])c1ccc(-c2nc3ccccc3s2)cc1
product
المردود 73.2%
O=[N+]([O-])c1ccc(-c2nc3ccccc3s2)cc1
2-(4-Nitrophenyl)benzothiazole
المردود 73.2%

الكواشف

لا شيء

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىThe reaction was quenched with water (20 mL)
  2. 2
    أخرىThe aqueous layer was separated
  3. 3
    استخلاصextracted with ethyl acetate (3×10 ml)
  4. 4
    أخرىThe combined organic layers were dried
  5. 5
    أخرىevaporated
  6. 6
    أخرىThe crude product was purified
  7. 7
    أخرىwith flush column, (hexane:ethyl acetate=85:15)

الإجراء التجريبي

A solution of 4-nitrobenzoyl chloride (1.49 g, 8.0 mmol) in benzene anhydrous, 10 mL) was added dropwise to 2-aminothiophenol (1.0 g, 8.0 mmol in 10 ml of benzene) at room temperature. The reaction mixture was allowed to stir for 16 hr. The reaction was quenched with water (20 mL). The aqueous layer was separated and extracted with ethyl acetate (3×10 ml). The combined organic layers were dried and evaporated. The crude product was purified with flush column, (hexane:ethyl acetate=85:15) to give 1.5 g (73.2%) of product as light yellow solid.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07351401B2uspto-grants-2008_04