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HRID 2099388作成日:2026年10月27日

3,4-dihydro-2H-pyran → 8-(tetrahydro-pyran-2-yloxymethyl)-3,4-dihydro-2H-naphthalen-1-one

https://huagongshe.com/reaction/2099388

反応式

関与物質

役割名称HCID仕込み量
反応物3,4-dihydro-2H-pyranHCID 8080—
反応物Benzenesulfonic acid, 4-methyl-, compd. with pyridine (1:1)HCID 466102—
反応物Sodium AcetateHCID 517045—
反応物HCID 178418287HCID 178418287—
溶媒DichloromethaneHCID 6344—
生成物8-(tetrahydro-pyran-2-yloxymethyl)-3,4-dihydro-2H-naphthalen-1-oneHCID 2198608955%

反応手順

The diol (Intermediate H3) (2.42 g, 13.5 mmol) was dissolved in CH2Cl2 (75 mL) and reacted with dihydropyran (1.3 mL, 13.8 mmol) and pyridinium para-toluene sulfonate (PPTS) (350 mg, 1.36 mmol) at rt for 18 h. The mixture was concentrated onto SiO2 and purified by chromatography with 10% EtOAc:Hx. The tetrahydropyranyl (THP) protected alcohol (2.02 g, 7.70 mmol) was dissolved in CH2Cl2 (10 mL) and added to a mixture of pyridinium chlorochromate (PCC) (4.9 g, 22.2 mmol), sodium acetate (310 mg, 3.56 mmol) and celite (110 g) in CH2Cl2 (100 mL). The mixture was reacted at rt for 18 h and filtered through celite. The residue was purified by chromatography on SiO2 with 20 to 30% EtOAc:Hx to yield 8-(tetrahydro-pyran-2-yloxymethyl)-3,4-dihydro-2H-naphthalen-1-one (Intermediate H4) (˜55%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07569584B2
出典データセットuspto-grants-2009_08
ORD IDord-f6c33da865724e7bb937be9df4336487
出典メモuspto-grants-2009_08