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HRID 393414作成日:2026年10月25日

Diisopropylamine → HCID 54128318、化合物

https://huagongshe.com/reaction/393414

反応式

関与物質

役割名称HCID仕込み量
反応物DiisopropylamineHCID 7912—
反応物HexaneHCID 8058—
反応物Ammonium ChlorideHCID 25517—
反応物Ethyl cyclopentanecarboxylateHCID 79550—
反応物4-Methoxybenzyl bromideHCID 165021—
反応物ButyllithiumHCID 178418339—
溶媒WaterHCID 962—
溶媒TetrahydrofuranHCID 8028—
溶媒Ethyl AcetateHCID 8857—
生成物HCID 54128318HCID 5412831879%

反応手順

A solution of diisopropylamine (58 mL, 0.44 mol) in THF 400 mL was cooled to below 0° C. and n-butyl lithium in hexane (170 mL, 2.5 N, 0.43 mol) was added dropwise maintaining the temperature below 0° C. Upon completion of the addition, ethyl cyclopentylcarboxylate (55 g, 0.39 mol) in THF (175 mL) was added dropwise maintaining the internal temperature between −60 and −70° C. Upon completion of the addition, the internal temperature was allowed to rise to −40° C. and was held there for 20 min and lowered back to −70° C. A solution of 4-methoxybenzyl bromide (75 g, 0.48 mol) in 175 mL of THF was added dropwise and the mixture was allowed to warm to room temperature overnight. A solution of 20% ammonium chloride in water (225 mL) was added followed by 450 mL of ethyl acetate, the layers were separated, the aqueous layer was extracted with ethyl acetate (450 mL) and the combined organic layers were washed with saturated brine (2×450 mL) and were dried (MgSO4). The crude product was chromatographed on silica gel, eluting with 1-5% ether in hexane to give 1-[(4-methoxyphenyl)methyl]cyclo-pentane carboxylic acid ethyl ester (80.8 g, 79%) as an oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06806365B2
出典データセットuspto-grants-2004_10
ORD IDord-48c227999ba04705ac8805d36c87507d
出典メモuspto-grants-2004_10