تفاعل #955900

ord-739e8ba836224e02a3ac2d1a3b3ef8dc

معادلة التفاعل

Oc1ccc(S)cc1
4-hydroxythiophenol
OCCBr
2-bromoethanol
O=C([O-])[O-].[K+].[K+]
K2CO3
OCCSc1ccc(O)cc1
(a)
المردود 72.0%

الكواشف

لا شيء

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    استخلاصextracted with dichloromethane (DCM) (3×50 ml)
  2. 2
    تجفيفThe organic part was dried by MgSO4
  3. 3
    أخرىsolvent was removed under a rotary evaporator
  4. 4
    أخرىThe crude product was purified on silica gel column

الإجراء التجريبي

(FIG. 2) (a) (4-(2-hydroxyethylsulfanyl) phenol) was synthesized by a modified literature procedure (pl add ref). 4-hydroxythiophenol (mercaptophenol) (6.00 g, 47.61 mmole), 2-bromoethanol (5.90 g, 47.6 mmol) and K2CO3 (6.6 g, 47.48 mmol) was stirred in dimethylformamide (DMF, 50 ml) at −5° C. for 30 minutes. The reaction mixture was then stirred for 12 hours at room temperature. The reaction mixture was poured in ice water (300 ml) and extracted with dichloromethane (DCM) (3×50 ml). The organic part was dried by MgSO4 and then solvent was removed under a rotary evaporator. The crude product was purified on silica gel column by using a chloroform/methanol (94:6) solvent mixture. Yield: 72%. 1H NMR (CDCl3): δ, 8.01 (s, OH, 1H), 7.33 (d, 2H, J=8.7 Hz), 6.78 (d, 2H, J=8.7 Hz), 4.52 (s, OH, 1H), 3.67 (t, 2H, J=6 Hz), 2.99 (t, 2H, J=5.7).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08968421B2uspto-grants-2015_03