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HRID 1109769作成日:2026年10月26日

Benzyl Alcohol → 3-(5-Fluorobenzothiazol-2-yl-trans-ethenyl)benzyl alcohol

https://huagongshe.com/reaction/1109769

反応式

関与物質

役割名称HCID仕込み量
反応物Benzyl AlcoholHCID 244—
反応物Acetic AnhydrideHCID 7918—
反応物IsophthalaldehydeHCID 34777—
反応物5-Fluoro-2-methylbenzothiazoleHCID 597437—
反応物Sodium borohydrideHCID 4311764—
反応物3-(5-Fluorobenzothiazol-2-yl-trans-ethenyl)benzaldehydeHCID 86747932—
触媒ZincchlorideHCID 3007855—
溶媒O-XyleneHCID 7237—
生成物3-(5-Fluorobenzothiazol-2-yl-trans-ethenyl)benzyl alcoholHCID 67828433—

反応手順

An alternate procedure for preparing this benzyl alcohol comprises condensing isophthalaldehyde with 2-methyl-5-fluorobenzothiazole in the presence of acetic anhydride and zinc chloride in hot xylene followed by the reduction of the 3-(5-fluorobenzothiazol-2-yl-trans-ethenyl)benzaldehyde product with sodium borohydride to provide the appropriate benzyl alcohol.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05322847
出典データセットuspto-grants-1994_06
ORD IDord-bebd70f669a54af8be82f17d90119462
出典メモuspto-grants-1994_06