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HRID 534001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/534001

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 1 N 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US08853409B2
出典データセットuspto-grants-2014_10
ORD IDord-b7c4027cdc354a2db8ea9cd6545bf4b5
出典メモuspto-grants-2014_10