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HRID 547849作成日:2026年10月24日

2,4-Dimethoxybenzyl alcohol → rac-(trans)-Cyclopentane-1,2-dicarboxylic acid mono-(2,4-dimethoxy-benzyl)ester

https://huagongshe.com/ja/reaction/547849

反応式

関与物質

役割名称HCID仕込み量
反応物2,4-Dimethoxybenzyl alcoholHCID 81750—
反応物1,2-Cyclopentanedicarboxylic acid, (1R,2R)-rel-HCID 727375—
反応物1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
触媒4-(Dimethylamino)pyridineHCID 14284—
溶媒WaterHCID 962—
溶媒DimethylformamideHCID 6228—
溶媒Sodium BicarbonateHCID 516892—
生成物rac-(trans)-Cyclopentane-1,2-dicarboxylic acid mono-(2,4-dimethoxy-benzyl)esterHCID 67153742—

反応手順

To a solution of (trans)-cyclopentane-1,2-dicarboxylic acid (1.90 g, 12 mmol), 2,4-dimethoxy-benzyl alcohol (2.02 g, 12 mmol), DMAP (73 mg, 0.6 mmol) in DMF (30 mL), chilled in an ice bath, was added EDC.HCl (2.53 g, 13.2 mmol) in two portions. The mixture was stirred at ice bath temperature for 15 min and warmed to RT for 4 hrs. The reaction mixture was diluted with H2O (100 mL) and saturated NaHCO3 (40 mL). The aqueous mixture was extracted with EtOAC (3×30 mL), acidified to pH 3 with saturated KHSO4 and extracted with EtOAc (3×30 mL). The combined organic layers were washed with H2O (2×25 mL), saturated NaCl (25 mL), dried over MgSO4, filtered and evaporated. The crude material was re-dissolved in CHCl3 and eluted through a silica gel plug with CHCl3 (100 mL) and then EtOAc (100 mL). The EtOAc fraction was evaporated and pumped to a clear oil, 2.6 g (70%), and used without further purification.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07939569B1
出典データセットuspto-grants-2011_05
ORD IDord-10ad6b1c511a486ba1fc2e1e9aec03bf
出典メモuspto-grants-2011_05