HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 990753Generated: October 30, 2026
Ammonium formate → HCID 18415746, compound
https://huagongshe.com/reaction/990753
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonium formate | HCID 2723923 | — |
| Reactant | HCID 18415760 | HCID 18415760 | — |
| Catalyst | Palladium hydroxide | HCID 9942167 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 18415746 | HCID 18415746 | 68% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06462035B1 |
|---|
| Source dataset | uspto-grants-2002_10 |
|---|
| ORD ID | ord-c8488cd98df7446eabab0b76fb5277fd |
|---|
| Source note | uspto-grants-2002_10 |
|---|