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HRID 2371498作成日:2026年10月25日

Iodoethane → Methyl(1-ethylinden-3-yl)acetate

https://huagongshe.com/reaction/2371498

反応式

関与物質

役割名称HCID仕込み量
反応物IodoethaneHCID 6340—
反応物Lithium diisopropylamideHCID 2724682—
反応物Methyl inden-3-ylacetateHCID 14316632—
溶媒TetrahydrofuranHCID 8028—
生成物Methyl(1-ethylinden-3-yl)acetateHCID 53874971—

反応条件

温度-70 °C

反応手順

To a solution of methyl inden-3-ylacetate from Example 13, Step 1 (1 g, 5.32 mmol) in THF (10 mL) at -70° C. was added dropwise a solution of LDA (12.2 mL, 0.87M, 2 eq.) in THF. The resulting orange solution was stirred for 30 minutes at -70° C. and then ethyl iodide (0.47 mL, 5.85 mmol) was added dropwise. The cooling bath was removed and the reaction mixture was left to warm to room temperature while a precipitate appeared. The reaction mixture was then quenched with a saturated aqueous solution of ammonium chloride and extracted with ethyl acetate. The organic layer was washed with 1N HCl, then with brine, dried over MgSO4 and evaporated to dryness. The 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-c5d06bfef23a4c0c9ce01f9763c05e82
出典メモuspto-grants-1992_03