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HRID 9294作成日:2026年10月24日

Hexamethylphosphoramide → 5-(2-Benzyloxy-ethyl)-2-oxo-cyclohexanecarboxylic acid methyl ester

https://huagongshe.com/ja/reaction/9294

反応式

関与物質

役割名称HCID仕込み量
反応物HexamethylphosphoramideHCID 12679—
反応物Carbonocyanidic acid, methyl esterHCID 28660—
反応物Lithium diisopropylamideHCID 2724682—
反応物4-(2-Benzyloxyethyl)cyclohexanoneHCID 21879605—
溶媒TetrahydrofuranHCID 8028—
生成物5-(2-Benzyloxy-ethyl)-2-oxo-cyclohexanecarboxylic acid methyl esterHCID 57443243—

反応条件

温度0 °C

反応手順

A solution of LDA (33 ml, 1.5 M in Et2O) in THF (50 mL) at −78° C. was treated with 4-(2-benzyloxy-ethyl)-cyclohexanone (9.5 g, 40.2 mmol). The mixture was warmed to 0° C. over 30 m before re-cooling to −78° C. and adding HMPA (7 mL). Methyl cyanoformate (4.1 mL, 85 mmol) was added and the mixture was stirred for 15 m before aqueous quench and work-up. The product was purified by chromatography on SiO2 with 10% EtOAc:Hx. 5-(2-Benzyloxy-ethyl)-2-oxo-cyclohexanecarboxylic acid methyl ester was isolated, 5.8 g (49%) and reduced with an equivalent of NaBH4 in MeOH at −10° C. to provide the alcohol (Intermediate R2). Intermediate R2 was purified by chromatography on SiO2 with 30 to 50% EtOAC:Hx. (˜90% yield).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07091232B2
出典データセットuspto-grants-2006_08
ORD IDord-36c0fb0cef9b4fd690399403bca865cf
出典メモuspto-grants-2006_08