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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1096192생성일: 2026년 10월 26일

1-Phenethylamine, (+)- → 2-(3-Chloro-4-trifluoromethyl-phenylamino)-propionic acid (r)-(+)-1-phenylethylamine salt

https://huagongshe.com/reaction/1096192

반응식

참여 물질

역할이름HCID투입량
반응물1-Phenethylamine, (+)-HCID 643189—
반응물HCID 66782716HCID 66782716—
용매Diisopropylether methanolHCID 21882575—
생성물2-(3-Chloro-4-trifluoromethyl-phenylamino)-propionic acid (r)-(+)-1-phenylethylamine saltHCID 8663837755.9%

반응 단계

A solution of (R)-(+)-1-phenylethylamine (104 mg, 0.86 mmol) in diisopropyl ether/MeOH 20:1 (4.5 mL) was added dropwise at RT to a solution of 2-(3-chloro-4-trifluoromethyl-phenylamino)-propionic acid (417 mg, 1.56 mmol) in diisopropyl ether/MeOH 20:1 (4.5 mL), then after 2 h the precipitate was collected by filtration, washed with diisopropyl ether, and dried under vacuum. This material was digested in chloroform (3 mL) at 50° C. for 18 h, then collected by filtration, and dried under vacuum to afford 2-(3-chloro-4-trifluoromethyl-phenylamino)-propionic acid (R)-(+)-1-phenylethylamine salt (187 mg). This salt was partitioned between 10% aq. KHSO4 solution and EtOAc. The organic layer was dried (MgSO4), filtered, and evaporated to afford the title compound (134 mg, 32%) in an enantiomeric ratio of 98.5:1.5. White solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08138175B2
출처 데이터셋uspto-grants-2012_03
ORD IDord-35e02b62ad7441899f74e26ace30d64e
출처 메모uspto-grants-2012_03