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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1752278Erstellt: 24. Oktober 2026

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

https://huagongshe.com/reaction/1752278

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt(R)-1-PhenylpropylamineHCID 5324978—
Edukt(R)-(+)-1-phenyl propyl ammonium (R)-(-)-chromane-2-carboxylateHCID 131733642—
LösungsmittelAcetonitrileHCID 6342—
Lösungsmitteltert-Butyl methyl etherHCID 15413—
Produkt(R)-chroman-2-carboxylic acidHCID 6933107—

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09163001B2
Quelldatensatzuspto-grants-2015_10
ORD IDord-e77e936cf70144a08a87af15ed098aee
Quellennotizuspto-grants-2015_10