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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1270240Generated: October 26, 2026

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

https://huagongshe.com/reaction/1270240

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 numberUS07202224B2
Source datasetuspto-grants-2007_04
ORD IDord-d9d6271a9335462c99a8c6f33e670764
Source noteuspto-grants-2007_04