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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1078569Generated: October 25, 2026

Thymine → 1-[(2-Acetoxyethoxy)Methyl]Thymine

https://huagongshe.com/reaction/1078569

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThymineHCID 1135—
ReactantTin tetrachlorideHCID 24287—
Reactant2-((Acetyloxy)methoxy)ethyl acetateHCID 100999—
ReactantSodium BicarbonateHCID 516892—
ReactantN,O-bis(trimethylsilyl)acetamideHCID 6913588—
SolventChloroformHCID 6212—
SolventDichloromethaneHCID 6344—
Product1-[(2-Acetoxyethoxy)Methyl]ThymineHCID 507887536%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05550132
Source datasetuspto-grants-1996_08
ORD IDord-fec2cfb7fb4e4c828b0878a20b1b5092
Source noteuspto-grants-1996_08