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HRID 1275511作成日:2026年10月25日

Methyl 4-iodosalicylate → Methyl 2-hydroxy-4-[3-hydroxy-3-(5,6,7,8-tetrahydro-3,5,5,8,8-pentamethyl-2-naphthyl)-1-propynyl]benzoate

https://huagongshe.com/reaction/1275511

反応式

関与物質

役割名称HCID仕込み量
反応物Methyl 4-iodosalicylateHCID 11380407—
反応物alpha-Ethynyl-5,6,7,8-tetrahydro-3,5,5,8,8-pentamethyl-2-naphthalenemethanolHCID 22361502—
生成物Methyl 2-hydroxy-4-[3-hydroxy-3-(5,6,7,8-tetrahydro-3,5,5,8,8-pentamethyl-2-naphthyl)-1-propynyl]benzoateHCID 2261942936.4%

反応手順

Following the basic procedure of Example 11(d), by reacting 1.28 g (5 mmol) of α-ethynyl-5,6,7,8-tetrahydro-3,5,5,8,8-pentamethyl-2-naphthalenemethanol [prepared in Example 37(d)] with 1.5 g (5.5 mmol) of methyl 2-hydroxy-4-iodobenzoate, 739 mg (36%) of the expected compound, with a melting point of 112°-113° C., were obtained.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06162445
出典データセットuspto-grants-2000_12
ORD IDord-83f53c638399404e89f83296e1a4596b
出典メモuspto-grants-2000_12