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HRID 22714作成日:2026年10月26日

Trimethyl orthoacetate → 5-Methoxy-2-methylbenzoxazole

https://huagongshe.com/reaction/22714

反応式

関与物質

役割名称HCID仕込み量
反応物Trimethyl orthoacetateHCID 15050—
反応物2-Amino-4-methoxyphenolHCID 1419108—
生成物5-Methoxy-2-methylbenzoxazoleHCID 79759—

反応手順

A solution of 2-amino-4-methoxyphenol 17 (8 g, 57.4 mmol) in trimethyl orthoacetate 18 (50 mL) was heated to reflux and allowed to stir for 24 h. The reaction was allowed to cool and the excess 18 was evaporated (in vacuo). The residue was dissolved in ethyl acetate and washed with water. The organic layer was dried over MgSO4 and treated with activated carbon Norit A. The resulting solution was filtered through Celite 521 and evaporated to yield an oil. The oil was chromatographed on silica gel (20% ethyl acetate/hexanes) to yield compound 19 as a light yellow solid. Synthesis of 2-methyl-5-oxiran-2-ylmethoxybenzoxazole (67):

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06849632B2
出典データセットuspto-grants-2005_02
ORD IDord-c0bca52f05014ddbbde713850ce9dfda
出典メモuspto-grants-2005_02