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HRID 222183作成日:2026年10月26日

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

https://huagongshe.com/reaction/222183

反応式

関与物質

役割名称HCID仕込み量
反応物Methyl iodideHCID 6328—
反応物Barium hydroxideHCID 6093286—
反応物Barium Oxide Nanoparticle DispersionHCID 9855530—
反応物tert-Butyl ((1R,2S)-2-hydroxy-2,3-dihydro-1H-inden-1-yl)carbamateHCID 17998891—
溶媒DimethylformamideHCID 6228—
生成物tert-Butyl [(1R,2S)-2-methoxy-2,3-dihydro-1H-inden-1-yl]carbamateHCID 8661425325%

反応手順

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 mL), 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 sodium bicarbonate and was extracted with DCM. The organic layer was washed with water (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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08207177B2
出典データセットuspto-grants-2012_06
ORD IDord-1e3564890bd74d739cb604b9b67590ff
出典メモuspto-grants-2012_06