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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 547849생성일: 2026년 10월 23일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물2,4-Dimethoxybenzyl alcoholHCID 81750—
반응물1,2-Cyclopentanedicarboxylic acid, (1R,2R)-rel-HCID 727375—
반응물1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
촉매4-(Dimethylamino)pyridineHCID 14284—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
용매Sodium BicarbonateHCID 516892—
생성물rac-(trans)-Cyclopentane-1,2-dicarboxylic acid mono-(2,4-dimethoxy-benzyl)esterHCID 67153742—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07939569B1
출처 데이터셋uspto-grants-2011_05
ORD IDord-10ad6b1c511a486ba1fc2e1e9aec03bf
출처 메모uspto-grants-2011_05