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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2308108Generated: November 2, 2026

Methyl iodide → HCID 60128538, compound

https://huagongshe.com/reaction/2308108

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
ReactantHCID 10331712HCID 10331712—
SolventTetrahydrofuranHCID 8028—
ProductHCID 60128538HCID 6012853828%

Reaction Steps

To a solution of benzyl (3R,4R)-3,4-dihydroxypyrrolidine-1-carboxylate (3.81 g, 16.1 mmol) in 60 mL THF was added NaH (0.803 g, 20.07 mmol). The reaction mixture was stirred at room temperature for 15 min, CH3I (2.0 mL, 32.2 mmol) was added and stirred at room temperature overnight. The reaction mixture was quenched with H2O (80 mL) and extracted with EtOAc (2×100 mL). The organic layer was dried and concentrated. The residue was purified by flash column chromatography (1˜2% CH3OH in CH2Cl2) to give a white solid (1.12 g, 28%). 1H NMR (CDCl3) δ 7.36-7.29 (5H, m), 5.12 (2H, s), 4.28-4.27 (1H, m), 3.72-3.37 (5H, m), 3.35 (3H, s), 1.95-1.89 (1H, m). ESIMS (MH+): 252.05.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06833456B2
Source datasetuspto-grants-2004_12
ORD IDord-a930792e358f4e39a19cd5e2b30c435a
Source noteuspto-grants-2004_12