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HRID 77908作成日:2026年10月24日

Ammonia → (4-(5-Methyl-furan-2-ylmethyl)-phenyl)-methanol

https://huagongshe.com/ja/reaction/77908

反応式

関与物質

役割名称HCID仕込み量
反応物AmmoniaHCID 222—
反応物LithiumHCID 3028194—
反応物Aluminum(III) ChlorideHCID 6451240—
反応物4-(Hydroxy-(5-methyl-furan-2-yl)-methyl)benzaldehydeHCID 59255336—
溶媒TetrahydrofuranHCID 8028—
生成物(4-(5-Methyl-furan-2-ylmethyl)-phenyl)-methanolHCID 59255234108.8%

反応手順

To a mixture of lithium aluminumhydride (230 mg, 4.9 mmol) and tetrahydrofuran (15 mL) was added aluminum chloride (830 mg, 6.2 mmol) at 0° C., which was stirred for 30 minutes at room temperature. A mixture of 4-(hydroxy-(5-methyl-furan-2-yl)-methyl)-benzaldehyde (320 mg, 1.5 mmol) described in Manufacturing Example 46-1-1 and tetrahydrofuran (5 mL) was added dropwise into the reaction mixture at 0° C., and stirred for 2 hours at that temperature. A 28% aqueous ammonia solution was added dropwise into the reaction mixture at the same temperature to quench the excess reagent. The reaction mixture was cooled to room temperature, and filtered by being passed through a Celite bed. The filtrate was concentrated under a reduced pressure to obtain the title compound (330 mg) as a crude product. This compound was used in the following reaction without further purification.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08841327B2
出典データセットuspto-grants-2014_09
ORD IDord-b0eb777ae6a74d7ea3169732f47b0d2e
出典メモuspto-grants-2014_09