戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 25483作成日:2026年10月26日

methyl (3R)-3-[(2-bromo-1-oxooctyl)oxy]-tetradecanoate → (2R)-5-hexyl-4-hydroxy-2-undecyl-2,3-dihydropyran-6-one

https://huagongshe.com/reaction/25483

反応式

関与物質

役割名称HCID仕込み量
反応物methyl (3R)-3-[(2-bromo-1-oxooctyl)oxy]-tetradecanoateHCID 11123443—
反応物HCID 178418310HCID 178418310—
溶媒TetrahydrofuranHCID 8028—
生成物(2R)-5-hexyl-4-hydroxy-2-undecyl-2,3-dihydropyran-6-oneHCID 5469002397%

反応手順

While the α-halo ester III and the reactive species generating reagent can be combined or added in any sequence, it has been found that when the reactive species generating reagent is a Grignard reagent a simultaneous addition of the α-halo ester III and the Grignard reagent is particularly preferred. For example, simultaneous addition of 13.6 mL solution of 30.7 mmol of methyl (3R)-3-[(2-bromo-1-oxooctyl)oxy]-tetradecanoate in tetrahydro-furan (THF) and 3 equivalents of tert-butyl magnesium chloride in 86 mL of THF over a one hour period to a 60° C. reaction vessel containing about 10 mL of THF solvent resulted in 97% yield (A.N., i.e., area normalized) of (6R)-3-hexyl-4-hydroxy-6-undecyl-5,6-dihydropyran-2-one when the crude product was analyzed by a gas chromatography 1 hr after the complete addition of reagents.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06858749B2
出典データセットuspto-grants-2005_02
ORD IDord-15f7ea4835ef4058bd5e2473fdec0a79
出典メモuspto-grants-2005_02