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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 870037생성일: 2026년 10월 23일

Tributylphosphine → 5-chloro-3-(3-chlorobenzyl)-N-[1-(4-cyanophenyl)ethyl]thiophene-2-carboxamide

https://huagongshe.com/ko/reaction/870037

반응식

참여 물질

역할이름HCID투입량
반응물TributylphosphineHCID 13831—
반응물Diphenyl diselenideHCID 15460—
반응물4'-CyanoacetophenoneHCID 74044—
반응물HCID 45140204HCID 45140204—
반응물HCID 57900982HCID 57900982—
용매AcetonitrileHCID 6342—
생성물5-chloro-3-(3-chlorobenzyl)-N-[1-(4-cyanophenyl)ethyl]thiophene-2-carboxamideHCID 57900981—

반응 단계

To a suspension of 5-chloro-3-(3-chlorobenzyl)thiopbene-2-carboxylic acid from Example 1, Step 6 (230 mg, 0.801 mmol), 4-(1-azidoethyl)benzonitrile (146 mg, 0.848 mmol) [prepared according to Thompson et al. J. Org. Chem. 1993, 58, 5886, after reduction of commercially available 4-acetylbenzonitrile] and diphenyl diselenide (549 mg, 1.76 mmol) in acetonitrile at r.t. under N2 was added tributylphosphine (217 μL, 0.881 mmol, 1.1 eq) dropwise (suspension dissolved, slightly exothermic) and the mixture was stirred at r.t. for 6 h, quenched with saturated NaHCO3 and extracted with ether. The crude was purified by Combi Flash chromatography system (10-40% EtOAc/hexane) to give the desired product.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08969394B2
출처 데이터셋uspto-grants-2015_03
ORD IDord-27512fc6ee68476f8bc87d3b9152fbd4
출처 메모uspto-grants-2015_03