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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2214533생성일: 2026년 10월 25일

Sodium Chloride → N-(3,4-Dichloro-benzyl)-2-(2,2-dimethyl-5-oxo-[1,3]dioxolan-4-ylidene)-N-methyl-acetamide

https://huagongshe.com/reaction/2214533

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참여 물질

역할이름HCID투입량
반응물Sodium ChlorideHCID 5234—
반응물Oxalyl chlorideHCID 65578—
반응물1-(3,4-Dichlorophenyl)-N-methylmethanamine hydrochlorideHCID 17293877—
반응물(2,2-Dimethyl-5-oxo-[1,3]dioxolan-4-ylidene)-acetic acidHCID 68860642—
용매BenzeneHCID 241—
용매Hydrochloric AcidHCID 313—
용매PyridineHCID 1049—
용매DichloromethaneHCID 6344—
생성물N-(3,4-Dichloro-benzyl)-2-(2,2-dimethyl-5-oxo-[1,3]dioxolan-4-ylidene)-N-methyl-acetamideHCID 6965573582%

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온도0 °C

반응 단계

To a suspension of (2,2-Dimethyl-5-oxo-[1,3]dioxolan-4-ylidene)-acetic acid, Compound III-A, (4.5 g, 26.2 mmol) in benzene (30 mL) was added oxalyl chloride (15 mL) and the resulting mixture was heated at reflux for 1 h. The mixture was cooled to room temp. and concentrated. The residue was dissolved in methylene chloride (30 mL) and cooled to 0° C. To this was added a suspension of (3,4-dichloro-benzyl)-methyl-amine hydrochloride salt (5.0 g, 22.1 mmol) in methylene chloride (30 mL) and pyridine (18 mL). The resulting mixture was stirred at room temp for 18 h then diluted with 1N HCl. The aqueous phase was saturated with sodium chloride and extracted with methylene chloride (3 times). The organic layers were combined, dried (Na2SO4), and concentrated. The brown oil was purified over silica gel eluting with ethyl acetate/hexane (1:1) to give the title compound as a pale yellow oil that solidified to a white solid upon standing (6.2 g, 82% yield). 1H NMR (300 MHz, DMSO) δ: 7.44–7.10 (m, 3H), 6.16 (s, 0.66H), 6.08 (s, 0.33H), 4.59 (s, 1.33H), 4.53 (s, 0.67H), 3.02 (s, 2H), 2.97 (s, 1H), 1.74 (s, 4H), 1.69 (s, 2H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07109186B2
출처 데이터셋uspto-grants-2006_09
ORD IDord-ca545db157cc491aace4a2e01517f5f2
출처 메모uspto-grants-2006_09