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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1616991Generated: November 2, 2026

Sodium Iodide → HCID 67534465, compound

https://huagongshe.com/reaction/1616991

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantHCID 86630303HCID 86630303—
SolventAcetoneHCID 180—
ProductHCID 67534465HCID 6753446579.6%

Reaction Steps

(2R,3R)-4,4-difluoro-5-(methylsulfonyloxy)-2-(trityloxymethyl)tetrahydrofuran-3-yl benzoate 9 (2 g, 3.37 mmol), acetone (20 mL), and NaI (5 g, 33.56 mmol) were charged into a round bottom flask. The resulting mixture was refluxed for >6 hours. HPLC indicated that all starting material 9 was consumed. The reaction mixture was cooled to ambient temperature and filtered. The solvent was removed in vacuo. The residue was partitioned between dichloromethane (105 mL) and water (65 mL). The aqueous layer was extracted with dichloromethane (30 mL). The combined dichloromethane layers were washed sequentially with a 5% aqueous solution of NaHSO3 (2×30 mL), a 1:1 mixture of water and brine (20 mL), and brine (2×20 mL). The solution was dried over MgSO4, filtered, and concentrated to give 1.68 g of (2R,3R)-4,4-difluoro-5-iodo-2-(trityloxymethyl)tetrahydrofuran-3-yl benzoate 10. H1 NMR (CDCl3): δ3.44-3.57 (dd, 2H), 4.41 (m, 1H), 5.60-5.65 (dd, 1H), 6.95 (d, 1H), 7.21-8.15 (m, 20H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08765933B2
Source datasetuspto-grants-2014_07
ORD IDord-c99ea5d853b049d7a168c7697893502e
Source noteuspto-grants-2014_07