反応 #351531

ord-80f75d592cbc471ca4fec0cd814319cc

反応方程式

Cl
hydrochloric acid
COC(=O)c1ccc(O)cc1O
methyl 2,4-dihydroxybenzoate
O=C([O-])[O-].[K+].[K+]
potassium carbonate
CCCCC(CC)CBr
2-ethylhexyl bromide
CCCCC(CC)COc1ccc(C(=O)OC)c(O)c1
methyl 4-(2-ethylhexyloxy)-2-hydroxybenzoate
収率 78.0%

反応条件

温度
80°CELSIUS
詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    workup.ADDITIONwas added
  2. 2
    その他dropwise at room temperature
  3. 3
    workup.ADDITIONAfter the dropwise addition
  4. 4
    抽出extracted with a 150 ml portion and two 50 ml portions of ethyl acetate
  5. 5
    抽出The resulting extract
  6. 6
    洗浄was washed successively with water
  7. 7
    乾燥a saturated sodium chloride aqueous solution, dried over anhydrous sodium sulfate
  8. 8
    濃縮concentrated
  9. 9
    その他to obtain a crude product
  10. 10
    その他The resultant crude product was purified by column chromatography

実験手順

To 30 ml of dimethylformamide (DMF) were added 5.00 g (29.9 mmol) of methyl 2,4-dihydroxybenzoate and 4.52 g (32.7 mmol) of potassium carbonate, and 6.32 g (32.7 mmol) of 2-ethylhexyl bromide was added thereto dropwise at room temperature. After the dropwise addition, the mixture was stirred at 80° C. for 5.5 hours. The reaction mixture was added to 200 ml of dilute hydrochloric acid and extracted with a 150 ml portion and two 50 ml portions of ethyl acetate. The resulting extract was washed successively with water and a saturated sodium chloride aqueous solution, dried over anhydrous sodium sulfate, and concentrated to obtain a crude product. The resultant crude product was purified by column chromatography to obtain 5.89 g (yield: 78%) of methyl 4-(2-ethylhexyloxy)-2-hydroxybenzoate represented by the following chemical formula (hereinafter referred to as compound 1) as a colorless, clear and oily substance. The analytical results of the product are shown below. ##STR22##

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US05646184uspto-grants-1997_07