戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 593394作成日:2026年10月26日

Methyl morpholine oxide → (3aR,6aS)-2-Oxo-3,3a,6,6a-tetrahydro-2H-cyclopenta[b]furan-5-carbaldehyde

https://huagongshe.com/reaction/593394

反応式

関与物質

役割名称HCID仕込み量
反応物Methyl morpholine oxideHCID 82029—
反応物(3aR,6aS)-2-Hydroxy-3,3a,6,6a-tetrahydro-2H-cyclopenta[b]furan-5-carbaldehydeHCID 72703147—
触媒HCID 178419074HCID 178419074—
溶媒DichloromethaneHCID 6344—
生成物(3aR,6aS)-2-Oxo-3,3a,6,6a-tetrahydro-2H-cyclopenta[b]furan-5-carbaldehydeHCID 9004973470%

反応手順

Purified lactol 7 (800 mg, 4.15 mmol), was dissolved in CH2Cl2 (52 ml) and stirred at r.t. 4-Methylmorpholine N-oxide (729 mg, 6.23 mmol) and 4 Å molecular sieve (2.8 g) were added as solids and the reaction mixture was stirred at r.t. for 10 min. Tetrapropylammonium perruthenate (146 mg, 0.415 mmol) was added as a solid and the reaction was stirred at r.t. for 14 hours. The reaction mixture was filtered over Celite® and the solids were washed with CH2Cl2 (3×10 ml). The organic phase was concentrated to give the crude material as a black oil. The material was purified by column chromatography eluting with CH2Cl2/EtOAc (9:1), to give the lactone 54, (439 mg, 70%) as a white solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09242954B2
出典データセットuspto-grants-2016_01
ORD IDord-078a0d48e576464aaab0e2a9dad86840
出典メモuspto-grants-2016_01