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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1684112Generated: November 2, 2026

Nitric Acid → HCID 10362873, compound

https://huagongshe.com/reaction/1684112

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitric AcidHCID 944—
ReactantHCID 10066058HCID 10066058—
ProductHCID 10362873HCID 10362873—

Reaction Conditions

Temperature0 °C

Reaction Steps

To 50 mL of red fuming nitric acid, chilled to 0° C., was added 2.3 g (6.69 mmol) of 30. After stirring at 0° C. for 45 minutes, 100 mL of ice water was added and the mixture quickly extracted with ethyl acetate. The ethyl acetate extract was dried over Na2SO4, evaporated down to a small volume, and placed on a silica gel column. Gradient chromatography (ethyl acetate to 5% methanolic ethyl acetate) afforded the desired product as a pure white solid: 1.5 g (58%) yield; TLC (ethyl acetate-methanol [9:1]), Rf =0,40; mp 259°-260° C.; IR (KBr pellet) 3370, 1676, 1651, 1568, 1534, 1472, 1404, 1373, 1315, 1054 cm-1 ; 1H NMR (dimethyl-d6 sulfoxide) δ9.99 (1H, s, acetamido proton), 8.64 and 8.28[2H, 2 s, J=2.3 Hz, 1- and 4-carbamyl protons, no assignments made), 4.25 (2H, s, methylene), 3.79 and 3.68 (6H, 2 s, 3- and 6-methoxys, no assignments made), 2.73 (6H, 2 overlapping d, J=4.4 Hz, 1- and 4-carbamyl methyls, no assignments made); mass spectrum (EI mode), m/z 388 (P+, 390 (P+, 37Cl).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05639881
Source datasetuspto-grants-1997_06
ORD IDord-2ded28312f5146e78a3beceecece5a46
Source noteuspto-grants-1997_06