HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2210896Erstellt: 25. Oktober 2026
Acetic Acid → 1-(Methoxymethyl)-6-phenylthiothymine
https://huagongshe.com/reaction/2210896
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Acetic Acid | HCID 176 | — |
| Edukt | Tetrahydrofuran | HCID 8028 | — |
| Edukt | Diphenyl disulfide | HCID 13436 | — |
| Edukt | Lithium diisopropylamide | HCID 2724682 | — |
| Edukt | 1-(Methoxymethyl)thymine | HCID 15042644 | — |
| Lösungsmittel | Ethyl Acetate | HCID 8857 | — |
| Produkt | 1-(Methoxymethyl)-6-phenylthiothymine | HCID 54016372 | 73% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US05461060 |
|---|
| Quelldatensatz | uspto-grants-1995_10 |
|---|
| ORD ID | ord-9025e083456c4fe890c080508c98be30 |
|---|
| Quellennotiz | uspto-grants-1995_10 |
|---|