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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1796300Generated: October 25, 2026

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

https://huagongshe.com/reaction/1796300

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 numberUS07030141B2
Source datasetuspto-grants-2006_04
ORD IDord-98e3e37385ea45d1b2b22d6f99d28bd8
Source noteuspto-grants-2006_04