تفاعل #1336

ord-78663f7332f8419998daa1598e9a7019

معادلة التفاعل

CCOC(=O)C1(O)CCC(C)(C)c2c1ccc(C#Cc1ccc(C(=O)OCC[Si](C)(C)C)cc1)c2C
trimethylsilylethyl 4-[(5,6,7,8-tetrahydro-5-hydroxy-8,8-dimethyl-5-carboethoxy-methylnaphth-2-yl)ethynyl]benzoate
CCOC(=O)C1(O)CCC(C)(C)c2c1ccc(C#Cc1ccc(C(=O)OCC[Si](C)(C)C)cc1)c2C
Compound 117
CCOC(=O)C1(O)CCC(C)(C)c2c1ccc(C#Cc1ccc(C(=O)OCC[Si](C)(C)C)cc1)c2C
trimethylsilylethyl 4-[(5,6,7,8-tetrahydro-5-hydroxy-8,8-dimethyl-5-carboethoxy-methylnaphth-2-yl)ethynyl]benzoate
CCCC[N+](CCCC)(CCCC)CCCC.[F-]
tetrabutyl ammonium fluoride
CCOC(=O)CC1(O)CCC(C)(C)c2cc(C#Cc3ccc(C(=O)O)cc3)ccc21
title compound
CCOC(=O)CC1(O)CCC(C)(C)c2cc(C#Cc3ccc(C(=O)O)cc3)ccc21
4-[(5,6,7,8-tetrahydro-5-hydroxy-8,8-dimethyl-5-carboethoxymethylnaphth-2-yl)ethynyl]benzoic acid

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    تركيزconcentrated in vacuo to an oil
  2. 2
    workup.ADDITIONslowly diluted with water
  3. 3
    استخلاصextracted with Et2O
  4. 4
    تجفيفThe organic layer was dried over Na2SO4
  5. 5
    تركيزconcentrated in vacuo to an oil
  6. 6
    أخرىpurified by flash chromatography (silica, 90% EtOAc-hexane)

الإجراء التجريبي

To a solution of 0.25 g (0.49 mmol) of trimethylsilylethyl 4-[(5,6,7,8-tetrahydro-5-hydroxy-8,8-dimethyl-5-carboethoxy-methylnaphth-2-yl)ethynyl]benzoate (Compound 117) in 5 ml of dry THF (flushed with argon) was added 1.48 ml (1.5 mmol) of tetrabutyl ammonium fluoride (1M solution in THF). The reaction mixture was stirred at room temperature for 12 hours, concentrated in vacuo to an oil and slowly diluted with water. The solution was acidified to pH 4 with 10% HCl and extracted with Et2O. The organic layer was dried over Na2SO4, concentrated in vacuo to an oil and purified by flash chromatography (silica, 90% EtOAc-hexane) to give the title compound as a white solid.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US05723620uspto-grants-1998_03