Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1738319Generated: November 4, 2026

Acetic Acid → (R)-3-(N-Cyclobutyl-N-n-propylamino)-8-fluoro-5-methoxy-3,4-dihydro-2H-1-benzopyran

https://huagongshe.com/reaction/1738319

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantPropanalHCID 527—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantHCID 53650127HCID 53650127—
SolventMethanolHCID 887—
Product(R)-3-(N-Cyclobutyl-N-n-propylamino)-8-fluoro-5-methoxy-3,4-dihydro-2H-1-benzopyranHCID 2287121880.6%

Reaction Steps

(R)-3-(N-Cyclobutylamino)-8-fluoro-5-methoxy-3,4-dihydro-2H-1-benzopyran (1.01 g, 4.02 mmol) was dissolved in anhydrous methanol (20 mL) and to this was n-propionaldehyde (3.0 mL, 40.2 mmol) added. After 1 h the reaction was cooled (ice-bath) then sodium cyanoborohydride (0.46 g, 7.24 mmol) was added, the pH was adjusted to 4-5 with acetic acid and the reaction was allowed to stir at room temperature over the weekend. The solvent was removed in vacuo, the remains were taken into a 2M solution of NH3 and then extracted thrice with diethyl ether. The combined ether portions were dried (MgSO4), filtered, and the solvent removed in vacuo to give the crude residue. Chromatography on silica (eluent 11% ethyl acetate/hexane) gave 0.95 g (80% yield) of the title compound as a clear oil. [α]21D =-95.4° (C=0.1; CHCl3). GC-MS (70 eV) M=293 (1%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05962514
Source datasetuspto-grants-1999_10
ORD IDord-562b0044ce9f48bca840c78f51e09d31
Source noteuspto-grants-1999_10