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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1752278생성일: 2026년 10월 25일

(R)-1-Phenylpropylamine → (R)-chroman-2-carboxylic acid

https://huagongshe.com/reaction/1752278

반응식

참여 물질

역할이름HCID투입량
반응물(R)-1-PhenylpropylamineHCID 5324978—
반응물(R)-(+)-1-phenyl propyl ammonium (R)-(-)-chromane-2-carboxylateHCID 131733642—
용매AcetonitrileHCID 6342—
용매tert-Butyl methyl etherHCID 15413—
생성물(R)-chroman-2-carboxylic acidHCID 6933107—

반응 단계

To a solution of Intermediate-1 (18.6 g, 104 mmol) in acetonitrile (91 mL), (R)-(+)-1-phenylpropylamine (9.14 g, 67.9 mmol) in methyl tert butyl ether (MTBE) (12 mL) solution was added in dropwise manner. After about half of the total amount of the (R)-(+)-1-phenylpropylamine solution was added. The reaction mixture was seeded with few crystals of ((R)-(+)-1-phenyl propyl ammonium (R)-(−)-chromane-2-carboxylate). The resultant thick slurry was diluted with MTBE (80 mL) and the mixture was further stirred for 6 h at RT. The salt was filtered, washed with MTBE and dried. The salt (13.7 g) was suspended in MTBE (80 mL) further aqueous HCl solution (1:1) (88 mL) was added and the mixture was stirred in cooling to 0° C. The aqueous layer was extracted with methyl tert-butyl ether (70 mL×2). The extracts were combined with organic layer and the solution was washed with 1:1 HCl solution (40 mL). The organic layer was dried over Na2SO4 and evaporated under reduced pressure to afford the title compound as a white crystalline solid (6.5 g); m/z-178.02.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09163001B2
출처 데이터셋uspto-grants-2015_10
ORD IDord-e77e936cf70144a08a87af15ed098aee
출처 메모uspto-grants-2015_10