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HRID 494568作成日:2026年10月26日

Cyclohexane, (bromomethyl)- → Methyl 3-cyclohexyl-2-methyl-2-phenylpropanate

https://huagongshe.com/reaction/494568

反応式

関与物質

役割名称HCID仕込み量
反応物Cyclohexane, (bromomethyl)-HCID 137636—
反応物Methyl alpha-methylbenzeneacetateHCID 569653—
反応物Lithium HexamethyldisilazideHCID 2733832—
溶媒TetrahydrofuranHCID 8028—
生成物Methyl 3-cyclohexyl-2-methyl-2-phenylpropanateHCID 6887455184.5%

反応条件

温度25 °C

反応手順

A solution of 2-phenyl-propionic acid methyl ester (3.0 g, 18.27 mmol) in tetrahydrofuran (25 mL) at −78° C. was treated dropwise with the lithium hexamethyldisilazide (21.9 mL, 1M in tetrahydrofuran, 21.9 mmol) and stirred for 1 hour. Bromomethyl-cyclohexane (3.09 mL, 21.92 mmol) was added to the reaction and the reaction was allowed to warm to 25° C. and stirred for 18 hours. The solvent was removed in vacuo and the residue was partitioned between water and ethyl acetate. The aqueous phase was extracted three times with ethyl acetate and the ethyl acetate layers were combined, dried with sodium sulfate, filtered, and concentrated in vacuo. The residue was chromatographed on silica gel eluting with hexane, then 2.5% ethyl acetate in hexane, and 5% ethyl acetate in hexane to give the title compound (4.02 g, 84%). 1H NMR (300 MHz, CDCl3): δ ppm 1.11 (m, 10H) 1.55 (m, 4H) 1.80 (m, 1H) 2.04 (m, 1H) 3.64 (m, 3H) 7.29 (m, 5H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07538105B2
出典データセットuspto-grants-2009_05
ORD IDord-ddfb2fe1ac2648dd89fd37fd398aae52
出典メモuspto-grants-2009_05