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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 222165Generated: October 31, 2026

Methyl iodide → HCID 66618095, compound

https://huagongshe.com/reaction/222165

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
Reactant1,1-Dimethylethyl N-[(1S)-2,3-dihydro-1H-inden-1-yl]carbamateHCID 86671904—
SolventTetrahydrofuranHCID 8028—
ProductHCID 66618095HCID 66618095—

Reaction Steps

To a solution of tert-butyl(1S)-2,3-dihydro-1H-inden-1-ylcarbamate (1.82 g, 7.80 mmol) in THF (50.0 mL) under an atmosphere of argon at 0° C. was added 60% sodium hydride in mineral oil (968 mg, 24.2 mmol) and the suspension was allowed to warm to rt and stir for 30 min. Iodomethane (1.52 mL, 24.2 mmol) was added and the mixture was stirred overnight. The reaction was then quenched via addition of saturated ammonium chloride solution (10.0 mL) and was concentrated in vacuo. The mixture was then partitioned between water (20 mL) and DCM (50 mL) and the aqueous layer was extracted with DCM (3×50 mL). The combined organic layers were dried over MgSO4, filtered, concentrated in vacuo and purified by silica gel chromatography eluting with a gradient of 0 to 20% EtOAc in hexanes to afford the title compound as a clear, colorless oil (1.84 g, 95%). LC/MS: Rt=2.21 min, ES+ 248 (AA standard).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08207177B2
Source datasetuspto-grants-2012_06
ORD IDord-b1b80948cbae4dc7891b01581cc6a5e7
Source noteuspto-grants-2012_06