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HRID 1064834作成日:2026年10月27日

Ammonium Chloride → 3-Methoxymethyloxy-1,2-benzenedimethanol

https://huagongshe.com/reaction/1064834

反応式

関与物質

役割名称HCID仕込み量
反応物Ammonium ChlorideHCID 25517—
反応物Aluminium lithium hydrideHCID 21226445—
反応物3-Methoxymethyloxyphthalic anhydrideHCID 21936735—
溶媒Diethyl EtherHCID 3283—
溶媒TetrahydrofuranHCID 8028—
生成物3-Methoxymethyloxy-1,2-benzenedimethanolHCID 2227285260%

反応手順

After that, lithium aluminum hydride (1.14 g, 30.0 mmol) was added little by little to a solution of 3-methoxymethyloxyphthalic anhydride (3.0 g, 14.4 mmol) in anhydrous tetrahydrofuran (100 ml) under cooling with ice water and the mixture was returned to room temperature followed by stirring for 12 hours. The reaction solution was diluted with ether (300 ml) and a saturated aqueous solution (3 ml) of ammonium chloride was added thereto followed by stirring for 1 hour. The reaction solution was dried over anhydrous magnesium sulfate, filtered off through celite and the filtrate was concentrated to provide 1.71 g (yield 60%) of 3-methoxymethyloxy-1,2-benzenedimethanol as colorless oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06969711B2
出典データセットuspto-grants-2005_11
ORD IDord-643fbb12b6c24edf9251de60c65dea63
出典メモuspto-grants-2005_11