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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 428345생성일: 2026년 10월 24일

Chlorotrimethylsilane → HCID 18357295, 화합물

https://huagongshe.com/ko/reaction/428345

반응식

참여 물질

역할이름HCID투입량
반응물ChlorotrimethylsilaneHCID 6397—
반응물N,N-Diisopropyl-3-(2-thienyl)propenamideHCID 4444087—
반응물HCID 178506687HCID 178506687—
용매Dimethyl SulfideHCID 1068—
용매Diethyl EtherHCID 3283—
생성물HCID 18357295HCID 18357295—

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06313132B1
출처 데이터셋uspto-grants-2001_11
ORD IDord-7d8c3fcafa8c48e68ccc416205efb9e8
출처 메모uspto-grants-2001_11