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HRID 15625作成日:2026年10月26日

Triphenylphosphine → 4-(4-Bromo-3,5-dimethylphenoxy)thiane

https://huagongshe.com/reaction/15625

反応式

関与物質

役割名称HCID仕込み量
反応物TriphenylphosphineHCID 11776—
反応物4-Bromo-3,5-dimethylphenolHCID 81970—
反応物ethyl N-ethoxycarbonyliminocarbamateHCID 220568—
反応物Tetrahydro-2H-thiopyran-4-olHCID 576296—
溶媒TetrahydrofuranHCID 8028—
生成物4-(4-Bromo-3,5-dimethylphenoxy)thianeHCID 5934255386.6%

反応手順

To a solution of 4-bromo-3,5-dimethylphenol (0.201 g, 1.00 mmol), tetrahydro-2H-thiopyran-4-ol (0.130 g, 1.10 mmol) and triphenylphosphine (0.341 g, 1.30 mmol) in tetrahydrofuran (5 mL) was added diethyl azodicarboxylate (40% solution in toluene, 0.591 mL, 1.30 mmol), and the mixture was stirred at room temperature for 1.5 hr. Tetrahydro-2H-thiopyran-4-ol (0.0591 g, 0.500 mmol), triphenylphosphine (0.157 g, 0.600 mmol) and diethyl azodicarboxylate (40% solution in toluene, 0.272 mL, 0.600 mmol) were added, and the mixture was further stirred for 1.5 hr. The reaction mixture was concentrated under reduced pressure, and the residue was purified by silica gel column chromatography (ethyl acetate:hexane=0:100-20:80) to give the title compound (0.261 g, yield 86%) as colorless crystals.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07732626B2
出典データセットuspto-grants-2010_06
ORD IDord-f048dd03d4064e58a82769102e031e02
出典メモuspto-grants-2010_06