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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 232728생성일: 2026년 10월 26일

4-(3-chlorophenyl)butanoic Acid → 6-Chloro-1-tetralone

https://huagongshe.com/reaction/232728

반응식

참여 물질

역할이름HCID투입량
반응물4-(3-chlorophenyl)butanoic AcidHCID 11321568—
용매Thionyl ChlorideHCID 24386—
생성물6-Chloro-1-tetraloneHCID 12291149—

반응 단계

A mixture of 35.72 of the product from Step B and 50 ml of thionyl chloride was heated at reflux for 2 hours and then stirred at room temperature for 18 hours. After this time thionyl chloride was removed at reduced pressure and the product was dissolved in carbon tetrachloride and concentrated at reduced pressure. The residue was dissolved in 150 ml of dichloroethane cooled to 0° C. and 28 g of aluminum chloride was added portionwise over about 1 hr in approximately 3 g portions. After stirring for 3 hrs the reaction was poured over a mixture of ice/1N HCl and extracted three times with methylene chloride. The organic extracts were dried over magnesium sulfate and concentrated to approximately 30 g of a brown oil. Chromatography on silica gel with 10% ethyl acetate/hexane afforded 17.83 g of 6-chloro-3,4-dihydro-1(2H)-naphthalenone as a brown oil. 1H NMR was consistent with the structure.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05591764
출처 데이터셋uspto-grants-1997_01
ORD IDord-bd72a0992b604eab8c6935803561f42f
출처 메모uspto-grants-1997_01