تفاعل #7998
ord-6ca20c97881a46a7b3a605c4a606073c
معادلة التفاعل
المتفاعلات
الكواشف
ظروف التفاعل
المعالجة
- 1درجة الحرارةAfter cooling
- 2ترشيحfiltered through a 0.45 Fm Acrodisc
- 3ترشيحfilter
- 4أخرىThe filtrate was evaporated under vacuum
- 5ترشيحthe residue in CH2Cl2 (3 mL) was re-filtered
- 6أخرىThe filtrate was purified by chromatography on a Biotage Flash 12M KP-Sil column (12 mm×15 cm) which
- 7غسيلwas eluted with 4:1 hexanes-EtOAc
- 8أخرىcollecting 6 mL fractions every 30 seconds
الإجراء التجريبي
A solution of 2-(2-methoxy-5-methyl-6-oxo-6,7,8,9-tetrahydro-8aH-fluoren-8a-yl)ethyl methanesulfonate (49.7 mg, 0.142 mmol) in acetone (2.0 mL) was treated with sodium iodide (85 mg, 0.57 mmol) and the resulting mixture was stirred and heated in an oil bath at 60° C. for 16 hours. After cooling, the mixture was diluted with acetone (2 mL) and filtered through a 0.45 Fm Acrodisc filter. The filtrate was evaporated under vacuum and the residue in CH2Cl2 (3 mL) was re-filtered. The filtrate was purified by chromatography on a Biotage Flash 12M KP-Sil column (12 mm×15 cm) which was eluted with 4:1 hexanes-EtOAc, collecting 6 mL fractions every 30 seconds. Fractions 9-11 gave 9a-(2-iodoethyl)-7-methoxy-4-methyl-1,2,9,9a-tetrahydro-3H-fluoren-3-one (34.5 mg, 64% yield) as an oil.