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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1523549생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/1523549

반응식

참여 물질

역할이름HCID투입량
반응물ChloroiodomethaneHCID 11644—
반응물Sodium HydroxideHCID 14798—
반응물Methyl (4S)-2,2-dimethyl-1,3-dioxolane-4-carboxylateHCID 853165—
반응물Lithium diisopropylamideHCID 2724682—
용매Acetic AcidHCID 176—
용매TetrahydrofuranHCID 8028—
용매Ethyl AcetateHCID 8857—
생성물(S)-2-chloro-1-(2,2-dimethyl-1,3-dioxolane-4-yl)ethanoneHCID 8664414842%

반응 조건

온도-78 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09079890B2
출처 데이터셋uspto-grants-2015_07
ORD IDord-31947033ea6a43b1869f04a67173fcd1
출처 메모uspto-grants-2015_07