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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1389823생성일: 2026년 10월 26일

Iodine → Ethyl 3-phenylindan-1-acetate

https://huagongshe.com/reaction/1389823

반응식

참여 물질

역할이름HCID투입량
반응물IodineHCID 807—
반응물Ethyl bromoacetateHCID 7748—
반응물1-Indanone, 3-phenyl-HCID 98146—
반응물Ethyl 3-phenylindene-1-acetateHCID 54109097—
촉매PalladiumHCID 23938—
촉매ZincHCID 23994—
용매Acetic AcidHCID 176—
용매BenzeneHCID 241—
용매WaterHCID 962—
용매Diethyl EtherHCID 3283—
생성물Ethyl 3-phenylindan-1-acetateHCID 12565675—

반응 단계

3-Phenyl-1-indanone (83 g, 0.4 mol) was dried by refluxing in C6H6 (120 ml) with removal of the azeotroped H2O. To this solution was added Et2O (120 ml) and Zn wool (26.25 g, 0.4 mol). The reaction mixture was heated to near reflux and a crystal of I2 added. Ethyl bromoacetate (110 g, 0.6 mol) was added over 2 hours, the temperature being kept near reflux by heat of reaction and some external heating. After the addition, the mixture was stirred and refluxed for a further 0.5 hour, cooled and poured into ice and acetic acid. The mixture was extracted with Et2O. The Et2O was washed with 1% NH4OH, dried (Na2SO4), filtered and evaporated and the residue distilled to give a mixture of ethyl 3-phenylindene-1-acetate and its corresponding double bond isomer (83.6g) b.p. 145°-155° C. (0.1 mm). This mixture of esters was hydrogenated over 10% Pd/C (0.6g) to give ethyl 3-phenylindan-1-acetate. This ester was hydrolyzed by refluxing with sodium hydroxide in ethanol to give the title compound, m.p. 126°-9° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04246281
출처 데이터셋uspto-grants-1981_01
ORD IDord-b553652ec8cd4a7f92aa2e1788d0cce0
출처 메모uspto-grants-1981_01