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HRID 129792作成日:2026年10月24日

Triphenylphosphine → HCID 19705817、化合物

https://huagongshe.com/ja/reaction/129792

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-PropylphenolHCID 12580—
反応物6-Bromo-1-hexanolHCID 77970—
反応物Diisopropyl azodicarboxylateHCID 5363146—
溶媒TetrahydrofuranHCID 8028—
生成物HCID 19705817HCID 1970581767%

反応手順

A solution of diisopropylazodicarboxylate (2.12 g, 10.5 mmol) in THF (25 mL) was added via syringe pump over 1.5 h to a mixture of 4-propylphenol (purchased from Aldrich Chemical Co.) (1.36 g, 10.0 mmol), 6-bromo-1-hexanol (purchased from Aldrich Chemical Co.) (1.81 g, 10.0 mmol), and triphenylphosphine (2.75 g, 10.5 mmol) in THF (25 mL) at 0° C. under argon. The slightly yellow reaction was stirred at 0° C. for 30 min, whereupon additional triphenylphosphine (262 mg, 1.00 mmol) was added, followed by addition of diisopropylazodicarboxylate (200 mL, 1.0 mmol) over 30 min. The reaction was allowed to warm to RT, at which time silica gel (15 g) was added. The mixture was concentrated in vacuo and the white powder obtained was purified by flash chromatography on silica gel (150 g) eluted with a step gradient of hexane to 2:98 EtOAc/hexane. The slightly impure product obtained was rechromatographed on silica gel (150 g) eluted with 1:99 EtOAc/hexane to give title compound (2.00 g, 67%) as a colorless oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05470845
出典データセットuspto-grants-1995_11
ORD IDord-7ec61da8bc61441bb34fb6ae35e507b0
出典メモuspto-grants-1995_11