تفاعل #586118

ord-33f16609e517490ebf38d9da5002e465

معادلة التفاعل

CCOCCOc1cc(C=O)cc2c1C(C)(C)CCC2(C)C
5,5,8,8-tetramethyl-4-(2-ethoxyethoxy)-5,6,7,8-tetrahydronaphthalene-2-carbaldehyde
C#[C][Mg][Br]
ethynylmagnesium bromide
C#CC(O)c1cc(OCCOCC)c2c(c1)C(C)(C)CCC2(C)C
1-[5,5,8,8-Tetramethyl-4-(2-ethoxyethoxy)-5,6,7,8-tetrahydronaphth-2-yl]prop-2-yn-1-ol
المردود 97.0%

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    استخلاصAfter treatment with 1N hydrochloric acid solution and extraction with ethyl acetate
  2. 2
    أخرىfollowed by evaporation
  3. 3
    أخرىthe residue is purified by chromatography on a column of silica (eluent: 8/2 heptane/EtOAC)
  4. 4
    أخرىA yellow oil is obtained (m=42 g; yield=97%)

الإجراء التجريبي

40 g (131 mmol) of 5,5,8,8-tetramethyl-4-(2-ethoxyethoxy)-5,6,7,8-tetrahydronaphthalene-2-carbaldehyde are dissolved in 400 mL of THF. 290 mL (145 mmol) of 0.5N ethynylmagnesium bromide solution are added and the reaction medium is then stirred for 1 hour. After treatment with 1N hydrochloric acid solution and extraction with ethyl acetate, followed by evaporation, the residue is purified by chromatography on a column of silica (eluent: 8/2 heptane/EtOAC). A yellow oil is obtained (m=42 g; yield=97%).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07767650B2uspto-grants-2010_08