تفاعل #82993
ord-de19ba1425fd497caef939f199f20c27
المتفاعلات
الكواشف
ظروف التفاعل
المعالجة
- 1أخرىto give a clear yellow solution
- 2أخرىto give a clear yellow solution
- 3أخرىThe tetrahydrofuran was removed by rotary evaporation
- 4ترشيحthe resulting solid filtered
- 5غسيلwashed with water
- 6workup.DISSOLUTIONredissolved in 10% NaOH
- 7ترشيحThis solution was filtered
- 8درجة الحرارةcooled
- 9أخرىreprecipitated with slow addition of HCl
- 10أخرىto give a yellow solid which
- 11ترشيحwas filtered
- 12غسيلwashed with water
- 13أخرىdried under vacuum
الإجراء التجريبي
To a suspension of 3,6-dihydroxyxanthone (46 g, 201 mmol.) obtained as in Example 1 in 1.6 L of THF was added over 1 hr 800 ml of borane-tetrahydrofuran complex (1.0M in THF, caution very vigorous raction at beginning). This mixture was stirred overnight under argon at room temperature to give a clear yellow solution. The excess diborane was decomposed by careful addition of water followed by 1N HCl to give a clear yellow solution. The tetrahydrofuran was removed by rotary evaporation and the resulting solid filtered, washed with water and redissolved in 10% NaOH. This solution was filtered, cooled and reprecipitated with slow addition of HCl to give a yellow solid which was filtered, washed with water and dried under vacuum to give 40.14 g (93%, mp 207-208) of 3,6-Dihydroxyxanthane. H1NMR (DMSO): 9.41 (s, 2H); 6.97 (d, 2H, J=8.4 Hz), 6.4 (dd, 2H, J=8.4, 2.4 Hz), 6.39 (d, 2H, J=2.4 Hz), 3.765 (s, 2H).