反応 #1121784

反応方程式

water

6-Benzyloxypurine

potasiumcarbonate

bromoacetic acid methyl ester

→

Methyl(6-(Benzyloxy)purin-9-yl)acetate

溶媒

DMF

butanol acetic acid water

ethylacetate

反応条件

後処理

1. 1
   乾燥The organic phase was dried over magnesium sulphate
2. 2
   その他evaporated to a volume of ˜10 ml
3. 3
   その他precipitated with pet. ether
4. 4
   その他The two products were separated by column chromatography
5. 5
   その他The products was precipitated in pet. ether

実験手順

6-Benzyloxypurine (4.18 g; 18.5 mmol) was added to a suspension of potasiumcarbonate (3.1 g; 22.4 mmol) in DMF (100 ml). After 15 min. bromoacetic acid methyl ester (1.93 ml; 20.4 mmol) was added. The reaction was monitored by TLC in butanol:acetic acid:water 4:1:1. Upon completion, the reaction mixture was portioned between water (600 ml) and ethylacetate (600 ml). The organic phase was dried over magnesium sulphate and evaporated to a volume of ˜10 ml and precipitated with pet. ether. The two products were separated by column chromatography using ethylacetate as the solvent. The products was precipitated in pet. ether. Yield: 2.36 g (43%). Melting point: 111.5-115° C. UV λmax=250 nm (9-alkylated); λmax=260 nm (7-alkylated). 1H-NMR (DMSO-d6): 8.60 (1H, s); 8.43 (1H, s); 7.6-7.35 (5H, m); 5.69 (2H, s); 5.26 (2H, s); 3.75 (3H, s).

出典