Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2210895Erstellt: 26. Oktober 2026

Thymine → 1-(Methoxymethyl)thymine

https://huagongshe.com/reaction/2210895

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktThymineHCID 1135—
EduktDichloromethaneHCID 6344—
EduktChloromethyl Methyl EtherHCID 7864—
EduktBistrimethylsilylacetamidHCID 11708267—
KatalysatorTetrabutylammonium IodideHCID 67553—
LösungsmittelMethanolHCID 887—
LösungsmittelWaterHCID 962—
Produkt1-(Methoxymethyl)thymineHCID 15042644—

Reaktionsschritte

To 250 ml of methylene chloride, 25 g (0.20 mol) of thymine and 109 ml (0.44 mol) of bistrimethylsilylacetamide were added under a nitrogen flow, and stirred for 2.5 hours at room temperature. To this mixture, 24 g (0.30 mole) of chloromethyl methyl ether and 0.59 g (1.6 mmol) of tetrabutylammonium iodide were added and heated under reflux for 1.5 hours. Then, the reaction mixture was added with 400 ml of methanol and 100 ml of water slowly and concentrated under reduced pressure. The residue was crystallized from ethyl acetate to obtain 1-(methoxymethyl)-thymine. Then, 119 ml of lithium diisopropylamide (0.25 mol) solution in tetrahydrofuran (2.1M) was added to 335 ml of tetrahydrofuran under a nitrogen flow at -70° C., to which a suspension of 17.0 g (0.10 mol) 1-(methoxymethyl)thymine in 107 ml of tetrahydrofuran was added dropwise over 30 minutes. After stirring for 2.5 hours at -70° C., the reaction mixture was added with a solution of 43.6 g of diphenyl disulfide in 49 ml of tetrahydrofuran dropwise over 20 minutes and allowed to react for 20 minutes. The reaction mixture was added with 35 ml of acetic acid, brought to room temperature and then added with 1 l of ethyl acetate. The mixture was washed with water (100 ml×5) and saturated solution of sodium hydrogencarbonate (twice), dried on magnesium sulfate and concentrated under reduced pressure. The residue was crystallized from ethanol to obtain 20 g of the target compound (Yield: 73%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05461060
Quelldatensatzuspto-grants-1995_10
ORD IDord-cacd7502c04b4a05a568272ea1335a84
Quellennotizuspto-grants-1995_10