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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 271268Generated: October 26, 2026

Ethyl bromoacetate → Ethyl 2,6-dichloro-9H-purine-9-acetate

https://huagongshe.com/reaction/271268

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl bromoacetateHCID 7748—
ReactantSodium hydrideHCID 24758—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 178478323HCID 178478323—
SolventTetrahydrofuranHCID 8028—
ProductEthyl 2,6-dichloro-9H-purine-9-acetateHCID 5810245953.1%

Reaction Conditions

Temperature0 °C

Reaction Steps

An ice-cold solution of 2,6-dichloro-1H-purine (1.89 g, 10 mmol) in THF (10 mL) was treated with NaH (60% in oil, 440 mg, 11 mmol), stirred at 0° C. for 30 min, treated with ethyl bromoacetate (1.22 mL, 11 mmol), stirred at room temperature for 2 h, poured into sat. NaHCO3, extracted with EtOAc and the combined organic phase dried (MgSO4), concentrated in vacuo and purified by chromatography [SiO2; Heptane:EtOAc (2:1)] to give the title compound (1.46 g, 53%) as a white solid: IR νmax (Nujol)/cm−1 3106, 2985, 2955, 2924, 2854, 1734, 1598, 1557, 1374, 1341, 1298, 1156 and 884; NMR δH (400 MHz, CDCl3) 1.31 (3H, t, J7.0 Hz), 4.29 (2H, q, J7.0 Hz), 5.01 (2H, s), 8.17 (1H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07452894B2
Source datasetuspto-grants-2008_11
ORD IDord-153185ed6827460b89ff207d8cb42b09
Source noteuspto-grants-2008_11