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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 23241Generated: October 27, 2026

Allyl bromide → 3'-O-Allyladenosine

https://huagongshe.com/reaction/23241

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
ReactantPhosphorus oxide (P4O10)HCID 14812—
ReactantSodium hydrideHCID 24758—
ReactantAdenosineHCID 60961—
SolventDimethylformamideHCID 6228—
Product3'-O-AllyladenosineHCID 1100129266%

Reaction Steps

Adenosine (20 g, 74.84 mmol) was dried over P2O5 under high vacuum at 40° C. for two days. It was then suspended in DMF under inert atmosphere. Sodium hydride (2.5 g, 74.84 mmol, 60% dispersion in mineral oil), stirred at room temperature for 10 minutes. Then allyl bromide (7.14 mL, 82.45 mmol) was added dropwise and the reaction mixture was stirred at room temperature overnight. DMF was removed under vacuum and residue was washed with ethyl acetate (100 mL). Ethyl acetate layer was decanted. Filtrate obtained contained product. It was then placed on a flash column and eluted with 10% MeOH in CH2Cl2 to get the title compound (15.19 g, 66%). Rf 0.4, 0.4a ((10% MeOH in CH2Cl2)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06849723B2
Source datasetuspto-grants-2005_02
ORD IDord-75b6f31520a04d588ebf5478b3981902
Source noteuspto-grants-2005_02