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HRID 337186作成日:2026年10月25日

Dichloromethane → Cyclohex-2-en-1-yl 2,2,2-trichloroethanimidate

https://huagongshe.com/reaction/337186

反応式

関与物質

役割名称HCID仕込み量
反応物DichloromethaneHCID 6344—
反応物TrichloroacetonitrileHCID 11011—
反応物2-Cyclohexen-1-OLHCID 13198—
生成物Cyclohex-2-en-1-yl 2,2,2-trichloroethanimidateHCID 13225936—

反応条件

温度-20 °C

反応手順

To a solution of 2-cylohexen-1-ol (16) (18 g, 0.183 mol) in dry dichloromethane (275 ml) DBU (41.88 g, 0.275 mol) was added and the mixture was cooled to −20° C. To this solution, trichloroacetonitrile (47.66 g, 0.330 mol) was added dropwise. The reaction was stirred for 3 h at −20° C. and quenched with aqueous ammonium chloride solution. The organic phase was separated and dried over potassium carbonate. The solvent was removed under vacuum to yield the intermediate cyclohex-2-en-1-yl 2,2,2-trichloroethanimidoate. This was dissolved in toluene (100 ml) and treated with potassium carbonate (30 g). The mixture was refluxed for 12 h. After cooling the mixture was filtered through Celite and the filtrate was evaporated to afford 9 g (20%) of (22) as a solid. LC/MS: Mass found (m/z, MS, 242.9) Method: A—0.1% HCOOH, B—ACN (70%), Flow-0.8 ml/min Column: GENESIS C18 50X4.6 mm 3 U, Rt (min): 1.645: 1H NMR (CDCl3, 400 MHz) δ 1.64-1.74 (3H, m), 1.96-2.12 (3H, m), 4.46-4.47 (1H, m), 5.64-5.67 (1H, m), 5.97-5.6.01 (1H, m), 6.59 (1H, bs).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08889719B2
出典データセットuspto-grants-2014_11
ORD IDord-4a35b879735a435d86e50074bc31ee66
出典メモuspto-grants-2014_11