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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2217583Generated: October 31, 2026

Methyl iodide → (2R,4R)-4-Methoxy-1-trityl-pyrrolidine-2-carboxylic acid methyl ester

https://huagongshe.com/reaction/2217583

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantEthyl AcetateHCID 8857—
ReactantSodium hydrideHCID 24758—
Reactant(2R,4R)-4-Hydroxy-1-trityl-pyrrolidine-2-carboxylic acid methyl esterHCID 68685802—
SolventDimethylformamideHCID 6228—
SolventTetrahydrofuranHCID 8028—
Product(2R,4R)-4-Methoxy-1-trityl-pyrrolidine-2-carboxylic acid methyl esterHCID 68806999—

Reaction Conditions

Temperature0 °C

Reaction Steps

Into a solution of 2 (5.71 g, 14.7 mmol) in anhydrous DMF (20 mL) and anhydrous THF (20 mL) was added MeI (3.67 mL, 58.9 mmol). The solution was cooled to 0° C. in an ice bath and NaH (0.766 g, 19.2 mmol) was added in one portion. The mixture was stirred at RT for 26 h before adding EtOAc and washing sequentially with water and brine. The organic layer was dried over MgSO4 and concentrated under reduced pressure. Purification of the crude material by flash chromatography revealed 3 (4.67 g, 79%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07407974B2
Source datasetuspto-grants-2008_08
ORD IDord-440eb8c0fa0b4d15bd0f30ef55c80560
Source noteuspto-grants-2008_08