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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 380127생성일: 2026년 10월 25일

Pipecolic Acid → 1-(3-Benzyloxybenzoyl)-2-piperidinecarboxylic acid

https://huagongshe.com/reaction/380127

반응식

참여 물질

역할이름HCID투입량
반응물Pipecolic AcidHCID 849—
반응물Isobutyl chloroformateHCID 62365—
반응물3-(Benzyloxy)benzoic acidHCID 309226—
반응물Sodium BicarbonateHCID 516892—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
용매TriethylamineHCID 8471—
생성물1-(3-Benzyloxybenzoyl)-2-piperidinecarboxylic acidHCID 1836741627%

반응 단계

Triethylamine (3.36 ml) was added to a stirred solution of 3-benzyloxybenzoic acid (5.0 g) and isobutyl chloroformate (3.13 ml) in THF (67 ml) under ice-cooling and the resulting mixture was stirred at the same temperature for 1 hour. A solution of 2-piperidinecarboxylic acid (4.14 g) and NaHCO3 (3.32 g) in water (40 ml) was added dropwise to the stirred mixture at the same temperature and the mixture was stirred at the same temperature for 2 hours and at room temperature overnight. The reaction mixture was partitioned between ethyl acetate and 1N HCl. The organic layer was separated, washed with 1N HCl (twice) and brine, dried over MgSO4, and evaporated in vacuo. The residue was chromatographed over silica gel to afford 1-(3-benzyloxybenzoyl)-2-piperidinecarboxylic acid (2.01 g) as a amorphous powder.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06300344B1
출처 데이터셋uspto-grants-2001_10
ORD IDord-729624d027f746eeb3938f65f3d118de
출처 메모uspto-grants-2001_10