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HRID 277976作成日:2026年10月26日

Benzyl Bromide → Benzyl 2-(3-methoxymethoxycarbonylnaphthalen-2-yl)benzoate

https://huagongshe.com/reaction/277976

反応式

関与物質

役割名称HCID仕込み量
反応物Benzyl BromideHCID 7498—
反応物Potassium CarbonateHCID 11430—
反応物2-(3-(Methoxymethoxycarbonyl)naphthalen-2-yl)benzoic acidHCID 17809303—
反応物Methoxymethyl 2-trifluoromethylsulfonyloxy-3-naphthalenecarboxylateHCID 22626196—
溶媒WaterHCID 962—
溶媒DimethylformamideHCID 6228—
生成物Benzyl 2-(3-methoxymethoxycarbonylnaphthalen-2-yl)benzoateHCID 22626517—

反応手順

Benzyl bromide (160 μl) and potassium carbonate (202 mg) were added to a solution of 2-(3-(methoxymethoxycarbonyl)naphthalen-2-yl)benzoic acid (410 mg) which was prepared by the same procedure as a series of reaction of Reference Example 4→Reference Example 5 using methoxymethyl 2-trifluoromethylsulfonyloxy-3-naphthalenecarboxylate, in dimethylformamid (5 ml). The mixture was stirred for 22 hours at room temperature. Water was added to the reaction mixture, and the solution was extracted with ethyl acetate. The extract was washed with water and a saturated aqueous solution of sodium chloride, successively, dried over anhydrous sodium sulfate and concentrated. The residue was purified by column chromatography on silica gel (hexane:ethyl acetate=8:2) to give the title compound (498 mg) having the following physical data.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06358960B1
出典データセットuspto-grants-2002_03
ORD IDord-fb38f4e051b74180a1a2d7e593c54025
出典メモuspto-grants-2002_03