تفاعل #1469
ord-223a80a8841041078a01144bb56456f4
معادلة التفاعل
ethyl(E)-4-[2-(5,5-dimethyl-5,6,-dihydro-naphthalen-8(7H)-one-2-yl)ethenyl]-benzoate
ethyl(E)-4-[2-(5,6-dihydro-5,5-dimethyl-naphthalen-8(7H)-one-2-yl)ethenyl]benzoate
Compound A2
ethyl(E)-4-[2-(5,6-dihydro-5,5-dimethyl-naphthalen-8(7H)-one-2-yl)ethenyl]benzoate
benzene
benzene
ethyl bromoacetate
→
title compound
(±)Ethyl (E)-4-[2-(5,6,7,8-tetrahydro-5,5-dimethyl-8-hydroxy-8-(methylcarbethoxy)naphthalen-2-yl)ethenyl]benzoate
المتفاعلات
الكواشف
ظروف التفاعل
الظروف التفصيلية
See reaction.notes.procedure_details.
المعالجة
- 1درجة الحرارةThe resulting mixture was refluxed for 24 h
- 2درجة الحرارةThe reaction was cooled
- 3ترشيحfiltered through celite
- 4غسيلThe filtrate was washed with 10% HCl, sat. aqueous NaHCO3 and brine
- 5تجفيفThe organic phase was dried over Na2SO4
- 6تركيزconcentrated in vacuo
- 7أخرىThe crude material was purified by flash chromatography (silica, 10% ethyl acetate in hexane)
الإجراء التجريبي
To a refluxing solution of 0.75 g (11.5 mmol) of granular zinc in 5.0 mL of benzene was added a solution of ethyl(E)-4-[2-(5,5-dimethyl-5,6,-dihydro-naphthalen-8(7H)-one-2-yl)ethenyl]-benzoate (Compound A2) in 5.0 mL of benzene followed by 0.27 g (0.18 mmol) of ethyl bromoacetate. The resulting mixture was refluxed for 24 h. The reaction was cooled, filtered through celite. The filtrate was washed with 10% HCl, sat. aqueous NaHCO3 and brine. The organic phase was dried over Na2SO4 and concentrated in vacuo. The crude material was purified by flash chromatography (silica, 10% ethyl acetate in hexane) to afford the title compound as a white solid.