Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2242469Generated: November 2, 2026

Acetone → HCID 14999717, compound

https://huagongshe.com/reaction/2242469

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
ReactantSodium CarbonateHCID 10340—
ReactantPerchloric AcidHCID 24247—
Reactant2-IodoadenosineHCID 169662—
ProductHCID 14999717HCID 1499971793%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a suspension of 2-iodoadenosine 1 (10.0 g, 25.4 mmol) in acetone (200 ml) cooled to 0° C. was added dropwise 70% perchloric acid (4.0 mL), resulting in an exotherm of about 5° C. The resultant colorless solution was allowed to warm to room temperature over 30 minutes, then stirred for a further 45 minutes. 1M Na2CO3 (50 mL) was added, resulting in solids precipitating. This was followed by the careful portionwise addition of water (300 mL) with stirring until all solids had dissolved. The mixture was extracted with three portions of CH2Cl2. The combined organics were washed with brine, dried (Na2SO4), filtered, and evaporated to afford Compound 2 (10.26 g, 93%) as a colorless solid. 1H-NMR (600 MHz, DMSO d6): 1.32 (s, 3H), 1.54 (s, 3H), 3.54 (m, 2H), 4.19 (m, 1H), 4.93 (dd, 1H), 5.05 (t, 1H), 5.27 (dd, 1H), 6.05 (d, 1H), 7.74 (bs, 2H), 8.28 (s, 1H); 13C-NMR (150 MHz, DMSO d6): 25.45, 27.08, 85.69, 86.09, 88.44, 92.59, 114.92, 120.39, 142.47, 151.08, 157.20, 173.14. LRMS (ES): m/z=434.0 (M+H, 100%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07671191B2
Source datasetuspto-grants-2010_03
ORD IDord-998afe3297a7493c99f2196b5715a74c
Source noteuspto-grants-2010_03