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HRID 2404375作成日:2026年10月26日

Ammonium Chloride → (1R,4R)-4-phenylcyclopent-2-enol

https://huagongshe.com/reaction/2404375

反応式

関与物質

役割名称HCID仕込み量
反応物Ammonium ChlorideHCID 25517—
反応物4-Cyclopentene-1,3-diol, 1-acetate, (1R,3S)-rel-HCID 9855498—
反応物HCID 178418546HCID 178418546—
反応物HCID 178478979HCID 178478979—
溶媒TetrahydrofuranHCID 8028—
生成物(1R,4R)-4-phenylcyclopent-2-enolHCID 1361383484%

反応手順

A solution of (1R,4S)-4-acetoxy-2-cyclopenten-1-ol (491 mg, 3.45 mmol), THF (10 mL), and copper(I) cyanide (93 mg, 1.04 mmol) was cooled to <−20° C. and phenylmagnesium chloride (2.0 M in THF, 5.18 mL, 10.4 mmol) was added at the same temperature. After 10 minutes, TLC (50% EtOAc/hexanes) showed complete conversion. Saturated aqueous NH4Cl (50 mL) was added, extracted with EtOAc (3×50 mL), and dried (Na2SO4) the combined organic layers. Concentrated and purified the residue by flash column chromatography (10-50% EtOAc/hexanes, gradient elution), to provide the title compound (463 mg, 2.89 mmol, 84%). MS (DCI) m/z 143 (M−OH)+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08802711B2
出典データセットuspto-grants-2014_08
ORD IDord-5fcbdfb42e2d4cc385125cd8f721f81d
出典メモuspto-grants-2014_08