HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1078569Generated: October 25, 2026
Thymine → 1-[(2-Acetoxyethoxy)Methyl]Thymine
https://huagongshe.com/reaction/1078569
Participants
| Role | Name | HCID | Charge |
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| Reactant | Thymine | HCID 1135 | — |
| Reactant | Tin tetrachloride | HCID 24287 | — |
| Reactant | 2-((Acetyloxy)methoxy)ethyl acetate | HCID 100999 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | N,O-bis(trimethylsilyl)acetamide | HCID 6913588 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-[(2-Acetoxyethoxy)Methyl]Thymine | HCID 5078875 | 36% |
Reaction Steps
Thymine (0.63 g, 5 mmol) was added to 2-acetoxyethyl acetoxymethyl ether (1.32 g, 7.5 mmol) dissolved in CH2Cl2 (15 mL). The reaction mixture was stirred at room temperature and N,O-bis(trimethylsilyl)acetamide (2.96 mL, 12 mmol) was added dropwise. After 3 hours of stirring, the clear solution was cooled to 0° C., and SnCl4 (0.12 mL, 1 mmol) was added. The reaction mixture was allowed to come to room temperature and stirred overnight. A mixture of saturated aqueous NaHCO3 (25 mL) and CHCl3 (50 mL) was prepared and cooled in ice. The reaction mixture was added slowly with vigorous stirring; a white foam formed immediately. After filtration, the aqueous layer was further extracted with ethyl acetate (3×25 mL) and CHCl3 (25 mL), and the combined organic layers were dried over anhydrous Na2SO4. After filtration of drying agent and removal of solvents in vacuo, an oily liquid was obtained. It was purified on a silica gel column using 2:1 CHCl3/CH3COCH3 as the eluent to give the desired product. Yield 36%; Wt. 4.0 g; mp 105°-107° C.; 1H NMR (DMSO-d6) 1.8 (s, CH3 C5 thymine), 2.0 (s, CH3 CO), 3.65 (m, CO O CH2 CH2), 4.1 (m, CO O CH2 CH2), 5.05 (s, O CH2 N), 7.55 (s, H C6 thymine), 11.3 (s, HN thymine ).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05550132 |
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| Source dataset | uspto-grants-1996_08 |
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| ORD ID | ord-fec2cfb7fb4e4c828b0878a20b1b5092 |
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| Source note | uspto-grants-1996_08 |
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