戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 379641作成日:2026年10月25日

Hydrochloric Acid → Methyl 2-methyl-3-(4-methylthiobenzyl)inden-1-ylacetate

https://huagongshe.com/reaction/379641

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物IodineHCID 807—
反応物Methyl bromoacetateHCID 60984—
反応物2-Methyl-3-(4-methylthiobenzyl)-1-indanoneHCID 18367456—
触媒ZincHCID 23994—
溶媒Diethyl EtherHCID 3283—
生成物Methyl 2-methyl-3-(4-methylthiobenzyl)inden-1-ylacetateHCID 18367447—

反応条件

温度0 °C

反応手順

To a solution of the indanone derivative from Step 1 (885 mg, 3.14 mmol) in ether (20 mL) were added successively zinc (840 mg, 12.8 mmol), methyl bromoacetate (0.5 mL, 5 mmol) and iodine (200 mg). The reaction mixture was refluxed for 3 hours, then cooled to 0° C. and 6N aqueous HCl was added dropwise until the zinc complex was completely decomposed. The organic layer was decanted, washed with brine, dried over Na2SO4 and evaporated to dryness. The oily residue was dissolved in formic acid and evaporated to dryness to complete the dehydration of the intermediate methyl [1-hydroxy-2-methyl-3-(4-methylthiobenzyl)indan-1-yl]acetate. The resulting oily residue was chromatographed on silica gel eluting with a 1:19 mixture of ethyl acetate-hexane to afford pure title compound as an oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06300346B1
出典データセットuspto-grants-2001_10
ORD IDord-3b1aab1c433143d5836a91946510fbde
出典メモuspto-grants-2001_10