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HRID 963882作成日:2026年10月26日

Water → Ethyl-6-[5,6,7,8-tetrahydro-5,5-dimethyl-8-(methoxymethyloxy)-naphth-7-yl]naphth-2-oate

https://huagongshe.com/reaction/963882

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物Chloromethyl Methyl EtherHCID 7864—
反応物DiisopropylethylamineHCID 81531—
反応物Ethyl 6-[5,6,7,8-tetrahydro-5,5-dimethyl-8-hydroxynaphth-2-yl]naphth-2-oateHCID 15462839—
反応物t-Butylammonium IodideHCID 22344722—
溶媒DichloromethaneHCID 6344—
溶媒Ethyl AcetateHCID 8857—
生成物Ethyl-6-[5,6,7,8-tetrahydro-5,5-dimethyl-8-(methoxymethyloxy)-naphth-7-yl]naphth-2-oateHCID 22571528—

反応手順

To a cold (0° C.) solution of 130 mg (0.35 mmol) of ethyl-6-[5,6,7,8-tetrahydro-5,5-dimethyl-8-(hydroxy)-naphth-7-yl]naphth-2-oate (Compound B4) in 2.0 mL of methylene chloride was added 50 mg (0.15 mL, 0.86 mmol) of Hunig's base, followed by 0.21 g (0.20 mL, 2.6 mmol) chloromethyl methyl ether was added and stirred at room temperature for 14 h. About 500 mgs of t-butylammonium iodide was then added and the reaction was warmed to 35° C. for one additional hour. The reaction was diluted with water, and extracted with CH2Cl2 (2×). The combined organic layer was washed with brine, dried over MgSO4, and concentrated in vacuo to give an oil. The title compound was obtained as an oil after flash chromatography (silica, 10 % ethyl acetate).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05763635
出典データセットuspto-grants-1998_06
ORD IDord-520b01a16fae450496f9530b4f0f95f5
出典メモuspto-grants-1998_06