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HRID 25153作成日:2026年10月26日

Bromocyclopentane → Tert-butyl 2-cyclopentyl-2-(4-methylphenyl)acetate

https://huagongshe.com/reaction/25153

反応式

関与物質

役割名称HCID仕込み量
反応物BromocyclopentaneHCID 8728—
反応物tert-Butyl (4-methylphenyl)acetateHCID 12362014—
反応物Potassium tert-butoxideHCID 23665647—
溶媒DimethylformamideHCID 6228—
生成物Tert-butyl 2-cyclopentyl-2-(4-methylphenyl)acetateHCID 15234721—

反応条件

温度0 °C

反応手順

33.5 g, (0.3 mol of potassium tert-butoxide are initially introduced into 100 ml of anhydrous DMF at 0° C., and 51.6 g (0.25 mol) of the compound from Example XX in 250 ml of anhydrous DMF are added dropwise. The mixture is stirred at 0° C. for 30 min and 32.2 ml (0.3 mol) of cyclopentyl bromide in 150 ml of anhydrous DMF are added dropwise at 5-15° C. and the mixture is stirred at 25° C. for 20 h. After concentrating, the residue is partitioned between water and diethyl ether, and the ether phase is dried over sodium sulphate and concentrated. The product crystallizes out.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06858622B2
出典データセットuspto-grants-2005_02
ORD IDord-f849e1c730c94e5db84ce2e7ae990baa
出典メモuspto-grants-2005_02