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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2273035Generated: November 1, 2026

HCID 14077945, compound → HCID 67481674, compound

https://huagongshe.com/reaction/2273035

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 14077945HCID 14077945—
CatalystNickelHCID 935—
SolventMethanolHCID 887—
SolventAmmonium HydroxideHCID 14923—
ProductHCID 67481674HCID 6748167481%

Reaction Steps

To a solution of rac-(2R,4aR,6R,7S,8R,8aR)-7-nitro-2-phenylhexahydro-4H-benzo[d][1,3]dioxine-6,8-diol (Carb. Res. 2002, 337, 1979-1992) (900 mg, 3.05 mmol) in MeOH (25 mL) and NH4OH (28% aqueous solution, 0.4 mL) was added Raney-Nickel (˜3 g). The mixture was hydrogenated at room temperature under atmosphere pressure for 20 h. The catalyst was filtered off and washed with MeOH. Solvents were evaporated to give the crude product. This was purified by silica gel chromatography, eluted with 15% MeOH in DCM and 83:14:3 DCM-MeOH-ammonia to give pure rac-(2R,4aR,6R,7S,8R,8aR)-7-amino-2-phenylhexahydro-4H-benzo[d][1,3]dioxine-6,8-diol (653 mg, 81%) as a white solid. 1H NMR (600 MHz, CD3OD) δ 7.52-7.50 (m, 2H), 7.37-7.32 (m, 3H), 5.58 (s, 1H), 4.13 (dd, J=11.0, 4.3, 1H), 3.68 (t, J=11.0, 1H), 3.51-3.41 (m, 3H), 2.67 (t, J=9.3, 1H), 1.83-1.76 (m, 2H), 1.17 (q, J=13.0, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09120781B2
Source datasetuspto-grants-2015_09
ORD IDord-aefe3208ac784f8cb1375dbb36d45ba6
Source noteuspto-grants-2015_09