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HRID 70519作成日:2026年10月23日

Triphenylphosphine → (R)-5-{[(1-phenyl-1H-tetrazol-5-yl)sulfanyl]methyl}pyrrolidin-2-one

https://huagongshe.com/ja/reaction/70519

反応式

関与物質

役割名称HCID仕込み量
反応物TriphenylphosphineHCID 11776—
反応物ethyl N-ethoxycarbonyliminocarbamateHCID 220568—
反応物(R)-(-)-5-(Hydroxymethyl)-2-pyrrolidinoneHCID 7128291—
反応物1-phenyltetrazole-5-thiolHCID 178527986—
溶媒WaterHCID 962—
溶媒TolueneHCID 1140—
溶媒TetrahydrofuranHCID 8028—
生成物(R)-5-{[(1-phenyl-1H-tetrazol-5-yl)sulfanyl]methyl}pyrrolidin-2-oneHCID 6739903918.4%

反応手順

1-Phenyl-1H-tetrazole-5-thiol (9.0 g) and triphenylphosphine (13.2 g) were added to a solution of (R)-(−)-5-(hydroxymethyl)-2-pyrrolidinone (4.5 g) in tetrahydrofuran (90 mL), followed by ice-cooling. A solution of 2.2 M diethyl azodicarboxylate in toluene (23 mL) was added dropwise thereto, and the mixture was stirred at room temperature overnight. The reaction solution was poured into water, followed by extraction with ethyl acetate. The organic layer was washed with brine, dried over anhydrous magnesium sulfate and filtered. The solvent was then evaporated under reduced pressure. The residue was purified by NH silica gel column chromatography (hexane:ethyl acetate=4:1→1:1→0:1) to give (R)-5-{[(1-phenyl-1H-tetrazol-5-yl)sulfanyl]methyl}pyrrolidin-2-one (1.98 g) as a colorless oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08822503B2
出典データセットuspto-grants-2014_09
ORD IDord-6e99fe8f850f46e2b4753643d346aefa
出典メモuspto-grants-2014_09