돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 9281생성일: 2026년 10월 24일

Oxalyl chloride → 1-Indanone, 4-bromo-

https://huagongshe.com/ko/reaction/9281

반응식

참여 물질

역할이름HCID투입량
반응물Oxalyl chlorideHCID 65578—
반응물3-(2-Bromophenyl)propionic acidHCID 316010—
반응물Aluminum(III) ChlorideHCID 6451240—
촉매DimethylformamideHCID 6228—
용매DichloromethaneHCID 6344—
생성물1-Indanone, 4-bromo-HCID 98713—

반응 조건

온도0 °C

반응 단계

4-Bromo-indan-1-one was obtained by the following procedure: A solution of 3-(2-bromo-phenyl)-propionic acid (commercially available from Oakwood Products) (15.0 g, 65.5 mmol) in CH2Cl2 at 0° C. was reacted with oxalyl chloride (7.2 mL, 1.5 eq) followed by 2–3 drops of DMF. The mixture was stirred until no more gas evolution was observed. As the mixture was concentrated and the residue was dissolved in CH2Cl2, cooled to 0° C., and treated with AlCl3 (9.6 g, 1.1 eq). After 1 h the mixture was quenched with water and the layers were separated. The aqueous layer was extracted with Et2O (3×150 mL) and the combined organic extracts were washed with H2O (3×100 mL), saturated NaHCO3 (3×100 mL), brine (1×100 mL), dried over MgSO4 and concentrated. 4-Bromoindan-1-one, 10.5 g (76%) was obtained by chromatography using 10% EtOAc:hexane as eluant. Use of 4-bromo-indan-1-one in Method NINETEEN produced 4-(4-bromo-indan-2-yl)-1,3-dihydro-imidazole-2-thione (Compound 149).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07091232B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-39187aa04b4741c7af65c404933627df
출처 메모uspto-grants-2006_08