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HRID 1523549作成日:2026年10月27日

Chloroiodomethane → (S)-2-chloro-1-(2,2-dimethyl-1,3-dioxolane-4-yl)ethanone

https://huagongshe.com/reaction/1523549

反応式

関与物質

役割名称HCID仕込み量
反応物ChloroiodomethaneHCID 11644—
反応物Sodium HydroxideHCID 14798—
反応物Methyl (4S)-2,2-dimethyl-1,3-dioxolane-4-carboxylateHCID 853165—
反応物Lithium diisopropylamideHCID 2724682—
溶媒Acetic AcidHCID 176—
溶媒TetrahydrofuranHCID 8028—
溶媒Ethyl AcetateHCID 8857—
生成物(S)-2-chloro-1-(2,2-dimethyl-1,3-dioxolane-4-yl)ethanoneHCID 8664414842%

反応条件

温度-78 °C

反応手順

To a solution of (S)-methyl 2,2-dimethyl-1,3-dioxolane-4-carboxylate (1.3 g, 8.1 mmol) and chloroiodomethane (4.3 g, 24 mmol) in THF (50 mL) at −78° C. was added a solution of LDA (16.2 mL, 24 mmol) in portions over 10 minutes. The reaction was stirred at −78° C. for 10 minutes. To this mixture was added a 10% solution of acetic acid (50 mL) in THF at −78° C. After addition, the slurry was warmed to ambient temperature. The reaction was poured into EtOAc (200 mL) and the aqueous layer basified using 1N NaOH. The organics were separated and washed with brine, dried over MgSO4 and concentrated in vacuo. The material was purified by chromatography using DCM as eluent to give (S)-2-chloro-1-(2,2-dimethyl-1,3-dioxolane-4-yl)ethanone (0.60 g, 3.4 mmol, 42% yield) as an oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09079890B2
出典データセットuspto-grants-2015_07
ORD IDord-31947033ea6a43b1869f04a67173fcd1
出典メモuspto-grants-2015_07