반응 #997158

ord-0c22fb64994b4963b3c3aaa28a14adde

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    workup.DISSOLUTIONdissolved in a 2 L three-neck flask
  2. 2
    기타equipped with a thermometer
  3. 3
    workup.ADDITIONwas gradually added
  4. 4
    workup.ADDITIONwas added
  5. 5
    세척washed 5 times
  6. 6
    추출The extraction liquid
  7. 7
    농축was concentrated

실험 절차

165 g (584 mmol) of 2-(2-(2-methyl-2-adamantyloxy)-2-oxoethoxy)-2-oxoethanol, 2,000 mL of THF, 105 mL (754 mmol) of triethylamine, and 0.165 g (1,000 ppm) of p-methoxyphenol were added to and dissolved in a 2 L three-neck flask equipped with a thermometer, a cooling pipe, and a stirring apparatus. After the dissolution, 62.7 mL (648 mmol) of methacryloyl chloride was gradually added thereto in an ice bath. Then, the resultant was heated at room temperature, and stirred for 3 hours. After the reaction, 1,000 mL of diethylether was added thereto, and then washed 5 times using 200 mL of distilled water. The extraction liquid was concentrated, thereby obtaining 198 g of the intended compound in the form of a colorless liquid (yield: 97%, GC purity: 99%).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US08021823B2uspto-grants-2011_09