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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 990753Generated: October 30, 2026

Ammonium formate → HCID 18415746, compound

https://huagongshe.com/reaction/990753

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium formateHCID 2723923—
ReactantHCID 18415760HCID 18415760—
CatalystPalladium hydroxideHCID 9942167—
SolventMethanolHCID 887—
ProductHCID 18415746HCID 1841574668%

Reaction Steps

11-Benzyl-5-Ethoxy-11-aza-tricyclo[7.3.1.02,7]trideca-2(7),3,5-triene hydrochloride (160 mg, mmol), ammonium formate (220 mg, 3.49 mmol) and 10%Pd(OH)2/C (100 mg) were combined in methanol (MeOH) (5 mL) and warmed to reflux for 15 min. The mixture was cooled, filtered, concentrated, diluted with sat. aq. Na2CO2 soln. and extracted with EtOAc (3×20 mL). The extracts were dried (MgSO4), filtered and concentrated to an oil (94 mg, 83%). (TLC 50%EtOAc/hexanes (NH3) Rf 0.20). 1H NMR (CDCl3) δ6.90 (d, J=9.0 Hz, 1H), 6.66 (2H), 3.97 (m, 2H), 3.08 (dd, J=18.0,6.0 Hz, 1H), 2.94 (m, 3H), 2.76-2.65 (3H), 1.96 (m, 2H), 1.88 (d, J=11.0 Hz, 1H), 1.38 (t, J=7.0 Hz, 3H). This material was dissolved in excess 1N HCl MeOH and concentrated. Recrystallization from CH2Cl2/Et2O provided a solid (74 mg, 68%). mp 243-245° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06462035B1
Source datasetuspto-grants-2002_10
ORD IDord-c8488cd98df7446eabab0b76fb5277fd
Source noteuspto-grants-2002_10