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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1618261Generated: October 30, 2026

Acetic Acid → HCID 66713284, compound

https://huagongshe.com/reaction/1618261

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantAmmoniaHCID 222—
ReactantSodium AzideHCID 33557—
ReactantHCID 66713131HCID 66713131—
SolventSulfuric AcidHCID 1118—
ProductHCID 66713284HCID 66713284—

Reaction Steps

[(1-Oxo-3-phenyl-1H-indene-2-carbonyl)-amino]-acetic acid methyl ester (1.864 g, 5.8 mmol) was dissolved in a mixture of concentrated H2SO4 (16 ml) and glacial acetic acid (16 ml) at 50 to 60° C. Then NaN3 (985 mg, 15 mmol) was added in portions with stirring so that the temperature did not exceed 60° C. Stirring was then continued at 50 to 60° C. for additional 30 min before the mixture was poured onto ice (200 g). The resulting mixture was basified by addition of concentrated aqueous NH3 (55 ml, D=0.89 g/ml) and extracted with CH2Cl2 (2×100 ml). The combined organic phases were dried over MgSO4 and then filtered through silica gel. The filtrate was discarded. The silica gel was washed with EtOAc (ca. 400 ml). The resulting solution was concentrated in vacuo to give a dark oil (250 mg). Further purification by flash column chromatography on silica gel using EtOAc and then EtOAc:hexanes=7:3 as the eluent gave the title compound as a tan solid (19 mg); 1H NMR (CDCl3): δ=7.11 to 7.98 (m), 3.75 (d, 2 H), 3.68 (s, 1H), 2.19 (s, 3 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08765956B2
Source datasetuspto-grants-2014_07
ORD IDord-75bc899acc234f8fab6919194353b787
Source noteuspto-grants-2014_07