Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 52260Generated: October 28, 2026

Ammonium formate → (R)-8-fluoro-5-methoxy-3-aminochroman

https://huagongshe.com/reaction/52260

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium formateHCID 2723923—
Reactant(R)-3-(N,N-Dibenzylamino)-8-fluoro-5-methoxy-3,4-dihydro-2H-1-benzopyranHCID 20640362—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
Product(R)-8-fluoro-5-methoxy-3-aminochromanHCID 2287121591.4%

Reaction Conditions

Temperature50 °C

Reaction Steps

(R)-3-(N,N-Dibenzylamino)-8-fluoro-5-methoxy-3,4-dihydro-2H-1-benzopyran (13.0 g, 34.4 mmol) was dissolved in 265 mL methanol and 115 mL THF. To this was 10% Pd/C (4 g) and ammonium formate (51.5 g, 0.817 mol) added. The reaction was heated to 50° C. for 2.5 h. The reaction was filtered and the solvent was removed in vacuo, the remains were taken into a 2 M solution of NaOH and then extracted twice with ether. The combined ether portions were treated with brine, dried (Na2SO4), filtered, and the solvent removed in vacuo to give 6.2 g (91% yield) of the title compound as a clear oil. [α]21D =-15.3° (C=1 CHCl3) GC-MS (70 eV) M=197 (51%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05616610
Source datasetuspto-grants-1997_04
ORD IDord-5873e019fbd4454a97065d1d92f5c096
Source noteuspto-grants-1997_04