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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 971148Generated: October 30, 2026

Methyl iodide → HCID 59020123, compound

https://huagongshe.com/reaction/971148

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantEthyl AcetateHCID 8857—
ReactantSodium hydrideHCID 24758—
Reactanttert-Butyl (1-(4-iodophenyl)cyclopropyl)carbamateHCID 59019959—
CatalystWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 59020123HCID 5902012395%

Reaction Steps

Part A. 1-(4-Iodophenyl)cyclopropyl-carbamic acid tert-butyl ester (2.14 g, 5.85 mmol) was stirred in THF (20 mL) at 0° C. under N2. MeI (3 mL) was added followed by portionwise addition of NaH (2.34 g, 5 eq). The reaction was stirred at rt overnight. Several drops of H2O and EtOAc (20 mL) were added to quench the reaction. The organic solvent was evaporated, and H2O was added. It was extracted with Et2O (2×), washed with brine, dried over MgSO4, and concentrated to dryness. The residue was purified by FCC (silica gel, CH2Cl2:hexanes=0:1 to 1:1 to 1:0) to give pure [1-(4-iodophenyl)cyclopropyl]-methyl-carbamic acid tert-butyl ester as a white solid (2.07 g, yield 95%). LC/MS (ESI+) 373.8 (M+H), tR=2.95 min (10–90% CH3CN in H2O in a 4-min run).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07312214B2
Source datasetuspto-grants-2007_12
ORD IDord-a401d52b00ca4ee092edf6dc12659914
Source noteuspto-grants-2007_12