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HRID 2371497作成日:2026年10月26日

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

https://huagongshe.com/reaction/2371497

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US05093356
出典データセットuspto-grants-1992_03
ORD IDord-2b2dee6f1c3241459509ee494d9a1377
出典メモuspto-grants-1992_03