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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 534001생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/534001

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 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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08853409B2
출처 데이터셋uspto-grants-2014_10
ORD IDord-b7c4027cdc354a2db8ea9cd6545bf4b5
출처 메모uspto-grants-2014_10