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HRID 1367716作成日:2026年10月25日

Iodine → Tetrahydro-2-(17-acetoxyheptadecyloxy)-2H-pyran

https://huagongshe.com/reaction/1367716

反応式

関与物質

役割名称HCID仕込み量
反応物IodineHCID 807—
反応物(S,S)-2,6-Bis(4-isopropyl-2-oxazolin-2-yl)pyridineHCID 688211—
反応物11-Bromoundecyl acetateHCID 5016162—
反応物2H-Pyran, tetrahydro-2-[(6-iodohexyl)oxy]-HCID 11056048—
触媒ZincHCID 23994—
触媒Dichloronickel;1,2-dimethoxyethaneHCID 15773433—
溶媒1,3-Dimethyl-2-imidazolidinoneHCID 6661—
溶媒TetrahydrofuranHCID 8028—
溶媒(R,R)-2,6-Bis(4-isopropyl-2-oxazolin-2-yl)pyridineHCID 688213—
生成物Tetrahydro-2-(17-acetoxyheptadecyloxy)-2H-pyranHCID 57548717—

反応条件

温度70 °C

反応手順

In a 10-ml Schlenk tube, zinc powder (98 mg, 1.5 mmol) was dried at 70° C. under high vacuum for 30 min. After back-filling with nitrogen, DMI (1 ml) and iodine (13 mg, 0.05 mmol) were added. The mixture was stirred until disappearance of the iodine color, after which neat 11-bromoundecyl acetate (293 mg, 1 mmol) was added. The tube was sealed, and the mixture was stirred at 70° C. for 12 h, cooled to the room temperature and zinc excess was allowed to settle. In a 5-ml flask, NiCl2-glyme (17 mg, 0.08 mmol) and (R)-(i-Pr)-Pybox (or (S)-(i-Pr)-Pybox) (30 mg, 0.1 mmol) were dissolved in DMI (1 ml) and THF (0.3 ml), then neat I(CH2)6OTHP 38 (240 mg, 0.77 mmol) was added followed by addition of the organozinc solution 33 via cannula. The reaction mixture was stirred at room temperature for 14 h, quenched with NH4Cl and extracted with EtOAc. The organic extract was dried over Na2SO4 and concentrated by solvent evaporation. Chromatography in hexane-ethyl ether (15:1, 10:1) gave the product, 212 mg (69%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07893286B2
出典データセットuspto-grants-2011_02
ORD IDord-3bc98490706f4cedae89a4779236c3f4
出典メモuspto-grants-2011_02