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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1245502Generated: October 26, 2026

Ethyl Acetate → 3'-Deoxy-5'-O-(4-methoxytrityl)-3'-(iodomethyl)-2'-O-(2-methoxyethyl)-5-methyluridine

https://huagongshe.com/reaction/1245502

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantDiisopropylethylamineHCID 81531—
Reactantp-Anisyldiphenylmethyl chlorideHCID 14836583—
Reactant3'-Deoxy-3'-(iodomethyl)-2'-O-(2-methoxyethyl)-5-methyluridineHCID 23518331—
SolventTetrahydrofuranHCID 8028—
Product3'-Deoxy-5'-O-(4-methoxytrityl)-3'-(iodomethyl)-2'-O-(2-methoxyethyl)-5-methyluridineHCID 23518332—

Reaction Steps

A mixture of 3′-deoxy-3′-(iodomethyl)-2′-O-(2-methoxyethyl)-5-methyluridine (472 mg, 1.1 mmol), diisopropylethylamine (0.79 mL, 0.586 g, 4.5 mmol), and p-anisyl chlorodiphenyl methane (4′-methoxytrityl chloride, MMT-Cl) (1.32 g, 4.27 mmol) in 6 mL of ethyl acetate and 4 mL of THF was stirred at rt for 48 h. The reaction mixture was diluted with ethyl acetate and washed with water, followed by brine. The organic phase was dried (Na2SO4) and concentrated. The crude product was purified by flash chromatography on a silica gel column. Gradient elution with 3:1, 2:1, 1:1, and then 1:3 hexanes-EtOAc provided 690 mg of the title compound as a white foam.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07125855B2
Source datasetuspto-grants-2006_10
ORD IDord-8081ff7c4e3b40729b4e056e00eb9d1a
Source noteuspto-grants-2006_10