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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
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
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| 反応物 | methyl (3R)-3-[(2-bromo-1-oxooctyl)oxy]-tetradecanoate | HCID 11123443 | — |
| 反応物 | HCID 178418310 | HCID 178418310 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | (2R)-5-hexyl-4-hydroxy-2-undecyl-2,3-dihydropyran-6-one | HCID 54690023 | 97% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US06858749B2 |
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| 出典データセット | uspto-grants-2005_02 |
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| ORD ID | ord-15f7ea4835ef4058bd5e2473fdec0a79 |
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| 出典メモ | uspto-grants-2005_02 |
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