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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1397516Generated: October 26, 2026

Methyl iodide → tert-Butyl [(1R,2S)-2-methoxy-2,3-dihydro-1H-inden-1-yl]carbamate

https://huagongshe.com/reaction/1397516

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantBarium hydroxideHCID 6093286—
ReactantBarium Oxide Nanoparticle DispersionHCID 9855530—
Reactanttert-Butyl ((1R,2S)-2-hydroxy-2,3-dihydro-1H-inden-1-yl)carbamateHCID 17998891—
SolventDimethylformamideHCID 6228—
Producttert-Butyl [(1R,2S)-2-methoxy-2,3-dihydro-1H-inden-1-yl]carbamateHCID 8661425325%

Reaction Steps

A mixture of tert-butyl [(1R,2S)-2-hydroxy-2,3-dihydro-1H-inden-1-yl]-carbamate (680. mg, 2.73 mmol), DMF (21.1), barium monoxide (5.02 g, 32.7 mmol), barium hydroxide (2.80 g, 16.4 mmol) and iodomethane (1.70 mL, 27.3 mmol) was stirred overnight. LC/MS showed no starting material. The reaction was quenched via addition of a saturated solution of NaHCO3 and was extracted with DCM. The organic layer was washed with H2O (3×), dried over sodium sulfate and concentrated in vacuo. The residue was purified via silica gel chromatography eluting with a gradient of 0 to 50% EtOAc in hexanes to afford the title compound (178 mg, 25%). LC/MS: Rt=1.24 min, ES+ 264 (AA standard).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08901136B2
Source datasetuspto-grants-2014_12
ORD IDord-9190c92a9bea446283485ea69d48174b
Source noteuspto-grants-2014_12