تفاعل #73527

ord-095d32159f074af9a6090351ff177e40

معادلة التفاعل

O=C(Cl)c1ccc(Cl)nc1
6-chloropyridine-3-carbonyl chloride
CC(C)(C)CO
2,2-dimethylpropanol
CC(C)(C)COC(=O)c1ccc(Cl)nc1
2,2-dimethylpropyl 6-chloropyridine-3-carboxylate
المردود 92.0%

الكواشف

لا شيء

المذيبات

ظروف التفاعل

درجة الحرارة
80°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةAfter cooling to room temperature
  2. 2
    تركيزthe medium is concentrated
  3. 3
    أخرىthe residue obtained
  4. 4
    غسيلwashed successively with water (2×200 mL), saturated NaHCO3 solution (2×200 mL) and brine (100 mL)
  5. 5
    تجفيفdried over Na2SO4
  6. 6
    تركيزconcentrated under reduced pressure
  7. 7
    أخرىpurified by chromatography on a column of silica gel
  8. 8
    غسيلeluting with a cyclohexane/EtOAc gradient of 0 to 5% EtOAc

الإجراء التجريبي

To a solution of 10 g (56.8 mmol) of 6-chloropyridine-3-carbonyl chloride in 100 mL of anhydrous toluene are added under argon, at room temperature, 15 g (170.4 mmol) of 2,2-dimethylpropanol. The reaction medium is then heated for 6 hours at 80° C. After cooling to room temperature, the medium is concentrated and the residue obtained is taken up in 800 mL of EtOAc, washed successively with water (2×200 mL), saturated NaHCO3 solution (2×200 mL) and brine (100 mL), dried over Na2SO4, and then concentrated under reduced pressure and purified by chromatography on a column of silica gel, eluting with a cyclohexane/EtOAc gradient of 0 to 5% EtOAc. 11.9 g of 2,2-dimethylpropyl 6-chloropyridine-3-carboxylate are obtained in the form of a white powder.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08541455B2uspto-grants-2013_09