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HRID 2214533作成日:2026年10月26日

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

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium ChlorideHCID 5234—
反応物Oxalyl chlorideHCID 65578—
反応物1-(3,4-Dichlorophenyl)-N-methylmethanamine hydrochlorideHCID 17293877—
反応物(2,2-Dimethyl-5-oxo-[1,3]dioxolan-4-ylidene)-acetic acidHCID 68860642—
溶媒BenzeneHCID 241—
溶媒Hydrochloric AcidHCID 313—
溶媒PyridineHCID 1049—
溶媒DichloromethaneHCID 6344—
生成物N-(3,4-Dichloro-benzyl)-2-(2,2-dimethyl-5-oxo-[1,3]dioxolan-4-ylidene)-N-methyl-acetamideHCID 6965573582%

反応条件

温度0 °C

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07109186B2
出典データセットuspto-grants-2006_09
ORD IDord-ca545db157cc491aace4a2e01517f5f2
出典メモuspto-grants-2006_09