Acetic Acid → 3-(5-Acetoxy-6-bromohexyl)-1-methylthymine
Reaction equation
[OH:1][CH:2]([CH2:17]O)[CH2:3][CH2:4][CH2:5][CH2:6][N:7]1[C:12](=[O:13])[C:11]([CH3:14])=[CH:10][N:9]([CH3:15])[C:8]1=[O:16].[BrH:19].[C:20]([OH:23])(=O)[CH3:21].C(=O)(O)[O-].[Na+]>ClCCl.O>[C:20]([O:1][CH:2]([CH2:17][Br:19])[CH2:3][CH2:4][CH2:5][CH2:6][N:7]1[C:12](=[O:13])[C:11]([CH3:14])=[CH:10][N:9]([CH3:15])[C:8]1=[O:16])(=[O:23])[CH3:21]Participants
Procedure
3-(5,6-Dihydroxyhexyl)-1-methylthymine (1.65 g, 6.4 mmol) was stirred with 30% hydrogen bromide in acetic acid (3.8 ml, 19.3 mmol) for 1.5 hours. The mixture was then added to a mixture of sodium bicarbonate (6.7 g), water (40 ml), and dichloromethane (50 ml). After 15 minutes of vigorous stirring, the layers were separated and the aqueous layer was extracted with dichloromethane (2×50 ml). The combined organic layers were dried over sodium sulfate and the solvent was evaporated under vacuum to give 3-(5-acetoxy-6-bromohexyl)- 1-methylthymine (2.30 g, 100% yield). The bromoacetate was used in the next step without further purification. 3-(5-Acetoxy-6-bromohexyl)-1-methylthymine (2.30 g, 6.4 mmol) was dissolved in methanol (10 ml) and a solution of 1M sodium methoxide in methanol (7 ml) was added. After stirring for 15 minutes, the solution was poured into water (60 ml) and extracted with 20% ethanol-dichloromethane (2×70 ml). The combined organic layers were dried over sodium sulfate and the solvents were evaporated under vacuum to give 3-(5,6-oxidohexyl)-1-methylthymine (1.30 g, 85% yield) as a white solid.
Workup
- customthe layers were separated
- extractionthe aqueous layer was extracted with dichloromethane (2×50 ml)
- dry with materialThe combined organic layers were dried over sodium sulfate
- customthe solvent was evaporated under vacuum
Sources & evidence
- ORD record
- ord-e928065a190146a78377ae2610d2874c
- Source dataset
- uspto-grants-1995_11
- Patent number
- US05470878
Reaction notes
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