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HRID 1994542作成日:2026年10月27日

Triethylamine → 4-[[[(1,1-Dimethylethyl)dimethylsilyl]oxy]methyl]thiazole

https://huagongshe.com/reaction/1994542

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物tert-Butyldimethylsilyl trifluoromethanesulphonateHCID 123564—
反応物(1,3-Thiazol-4-yl)methanolHCID 2763215—
溶媒DichloromethaneHCID 6344—
溶媒Ethyl AcetateHCID 8857—
生成物4-[[[(1,1-Dimethylethyl)dimethylsilyl]oxy]methyl]thiazoleHCID 66716662—

反応条件

温度-78 °C

反応手順

To a solution of 1,3-thiazol-4-ylmethanol (311.4 mg, 2.7 mmol) in CH2Cl2 (15 mL) was added Et3N (1.9 mL, 13.6 mmol). The solution was cooled to −78° C. and TBSOTf (776 μL, 3.38 mmol) was added. The reaction was warmed to room temperature and stirred for 1 hour. Next, the reaction was diluted with EtOAc (75 mL) and washed with saturated NaHCO3, brine, 1N HCl, and brine (20 mL each). The organic layer was dried over Na2SO4, filtered, and concentrated. The residue was purified by flash chromatography on silica gel (0 to 15% EtOAc/hexanes) to afford 4-({[tert-butyl(dimethyl)silyl]oxy}methyl)-1,3-thiazole. Rf=0.28 (15% EtOAc/hexanes). LCMS=230.1 (M+1)+. 1H NMR (CDCl3, 600 MHz) δ 8.77 (d, J=2.0 Hz, 1H), 7.25 (m, 1H), 4.93 (d, J=1.1 Hz, 2H), 0.95 (s, 9H), 0.12 (s, 6H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07652049B2
出典データセットuspto-grants-2010_01
ORD IDord-2a99fa1f3a634d1eb48ca5ea284c46c6
出典メモuspto-grants-2010_01