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HRID 428345作成日:2026年10月26日

Chlorotrimethylsilane → N,N-Diisopropyl-3-(2-methoxyphenyl)-3-(2-thienyl)propanamide

https://huagongshe.com/reaction/428345

反応式

関与物質

役割名称HCID仕込み量
反応物ChlorotrimethylsilaneHCID 6397—
反応物N,N-Diisopropyl-3-(2-thienyl)propenamideHCID 4444087—
反応物HCID 178506687HCID 178506687—
溶媒Dimethyl SulfideHCID 1068—
溶媒Diethyl EtherHCID 3283—
生成物N,N-Diisopropyl-3-(2-methoxyphenyl)-3-(2-thienyl)propanamideHCID 18357295—

反応手順

Copper(I)bromide dimethyl sulfide complex (4.63 g 22.5 mmol) was dissolved in dimethyl sulfide (18 mL), and diethyl ether (15 mL). The solution was cooled to 0° C., whereafter 2-methoxyphenyllithium (41.2) (45 mmol) was added. After 10 min., the temperature was lowered to −78° C. Trimethylsilylchloride (4.89 g, 45.0 mmol) was added, followed by N,N-diisopropyl-3-(2-thienyl)propenamide (41.1) (3.56 g, 15 mmol) in diethyl ether (20 mL). The temperature was allowed to slowly rise to room temperature overnight. The reaction was quenched with saturated NH4Cl (10 mL) and conc. ammonia (10 mL). Diethyl ether (80 mL) was added and the mixture was filtered through Celite. The aqueous phase was extracted twice with diethyl ether. The combined organic phases were washed once with brine and dried (MgSO4). The solvent was evaporated and the crude product was chromatographed on silica (petroleum ether-ethyl acetate 3:1), affording a yellow oil, 3.75 g (73%): 1H NMR (CDCl3) d 1.12 (t, 6H), 1.29 (t, 6H), 3.02 (m, 2H), 3.4 (br, 1H), 3.80 (s, 3H), 4.03 (m, 1H), 5.26 (t, 1H), 6.8-7.3 (m, 7H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06313132B1
出典データセットuspto-grants-2001_11
ORD IDord-7d8c3fcafa8c48e68ccc416205efb9e8
出典メモuspto-grants-2001_11