戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1389823作成日:2026年10月27日

Iodine → Ethyl 3-phenylindan-1-acetate

https://huagongshe.com/reaction/1389823

反応式

関与物質

役割名称HCID仕込み量
反応物IodineHCID 807—
反応物Ethyl bromoacetateHCID 7748—
反応物1-Indanone, 3-phenyl-HCID 98146—
反応物Ethyl 3-phenylindene-1-acetateHCID 54109097—
触媒PalladiumHCID 23938—
触媒ZincHCID 23994—
溶媒Acetic AcidHCID 176—
溶媒BenzeneHCID 241—
溶媒WaterHCID 962—
溶媒Diethyl EtherHCID 3283—
生成物Ethyl 3-phenylindan-1-acetateHCID 12565675—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04246281
出典データセットuspto-grants-1981_01
ORD IDord-b553652ec8cd4a7f92aa2e1788d0cce0
出典メモuspto-grants-1981_01