反応 #5107

ord-d238f04b14bc48fe99e1c99449a0250c

反応方程式

CC(C)(C)c1ccc(OCCCCO)cc1
4-p-t-butylphenoxy-1-butanol
O=C(O)c1cccnc1
nicotinic acid
O=S(Cl)Cl
thionyl chloride
O=C(Cl)c1cccnc1
Nicotinoyl chloride

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    温度at reflux for two hours
  2. 2
    その他The excess thionyl chloride was removed in vacuo
  3. 3
    洗浄After forty-eight hours the mixture was washed with one liter of saturated sodium bicarbonate
  4. 4
    乾燥The dichloromethane solution was dried over magnesium sulfate
  5. 5
    その他evaporated to a syrupy residue
  6. 6
    その他The material was chromatographed on 1 kg of silica gel with elution by dichloromethane-methanol, 96:4

実験手順

Nicotinoyl chloride was prepared by treating 100 g (0.81 mole) of nicotinic acid with 280 ml of thionyl chloride at reflux for two hours. The excess thionyl chloride was removed in vacuo and the crystalline acid chloride hydrochloride was suspended in 500 ml of dichloromethane. To the stirred mixture was added 66 g (0.30 mole) of 4-p-t-butylphenoxy-1-butanol dissolved in 400 ml of dichloromethane. After forty-eight hours the mixture was washed with one liter of saturated sodium bicarbonate. The dichloromethane solution was dried over magnesium sulfate and evaporated to a syrupy residue. The material was chromatographed on 1 kg of silica gel with elution by dichloromethane-methanol, 96:4, to afford 43.8 g (45%) of the nicotinate ester as an oil. The hydrobromide salt was prepared by treatment of a solution of 43.8 g in 800 ml of ethyl acetate with 30 ml of 4.5N hydrogen bromide in ether. The precipitate was collected, washed with pentane and dried, m.p. 132°-133° C.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US05242936uspto-grants-1993_09