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HRID 646816作成日:2026年10月26日

Methyl iodide → Ethyl 2-(4-methylphenyl)propanoate

https://huagongshe.com/reaction/646816

反応式

関与物質

役割名称HCID仕込み量
反応物Methyl iodideHCID 6328—
反応物Ethyl p-tolylacetateHCID 84175—
反応物Benzeneacetic acid, alpha-methyl-, ethyl esterHCID 99643—
反応物Lithium diisopropylamideHCID 2724682—
溶媒TetrahydrofuranHCID 8028—
溶媒2(1H)-Pyrimidinone, tetrahydro-1,3-dimethyl-HCID 81646—
生成物Ethyl 2-(4-methylphenyl)propanoateHCID 1107052486%

反応手順

According to the procedure given for the synthesis of 202, ethyl p-tolylacetate (2.72 g, 15.2 mmol) was reacted with LDA (7.6 mL, 15.25 mmol) and methyl iodide (3.03 g, 21.30 mmol) in anhydrous THF (70 mL) and DMPU (1 mL). After aqueous workup and extraction, the residue was distilled in high vacuo to give 203 (2.5 g, 86.0%) as an oil. Bp 59-63° C./0.2 mmHg. 1H NMR (CDCl3): δ (ppm) 7.18 (d, 2H, J=8.1), 7.10 (d, 2H, J=8.1), 4.09 (m, 2H), 3.61 (q, 1H, J=7.2), 2.29 (s, 3H), 1.47 (d, J=7.2 Hz, 3H), 1.20 (t, J=5.7 Hz, 3H). 13C NMR (75 MHz, CDCl3/TMS): δ (ppm) 174.71, 137.80, 136.63, 129.33, 129.14, 127.36, 60.66, 45.18, 21.05, 18.70, 14.15.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07705177B2
出典データセットuspto-grants-2010_04
ORD IDord-f03e46c567c145b1a4076a5e652005a2
出典メモuspto-grants-2010_04