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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1444774Generated: November 1, 2026

Ethyl Acetate → HCID 86589703, compound

https://huagongshe.com/reaction/1444774

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantBenzene, 1-(chloromethyl)-3,5-dinitro-HCID 94673—
ReactantSodium BromideHCID 253881—
Reactant2,3,3-trimethyl-3H-indol-5-yl-acetic acidHCID 14117637—
SolventSulfolaneHCID 31347—
ProductHCID 86589703HCID 8658970354%

Reaction Conditions

Temperature100 °C

Reaction Steps

3,5-Dinitrobenzyl chloride (12.46 g, 57.5 mmol) was added to a solution of 2,3,3-trimethyl-3H-indol-5-yl-acetic acid (2.5 g, 11.5 mmol) with sodium bromide (5.92 g, 57.5 mmol) in sulfolan (10 ml). The reaction was heated at 100° C. for 20 hrs, then cooled to room temperature. The crude reaction mixture was added dropwise to an excess of ethyl acetate and the dark brown solid was filtered OFF and dissolved in dimethylsulfoxide before purification by reverse phase chromatography. The product was isolated as beige solid (54% yield). 1H NMR (d6-DMSO): δH: 8.75 (s, 1H), 8.45 (s, 2H), 7.15 (s, 1H), 6.95 (d, 1H), 6.70 (d, 2H), 5.10 (s, 2H), 3.95 (s, 2H), 3.45 (s, 3H), 1.40 (s, 6H). MALDI-TOF, m/z=398 (M+=398 for C20H20N3O6).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07662973B2
Source datasetuspto-grants-2010_02
ORD IDord-d963380559a442ea9a4521d29c994e4f
Source noteuspto-grants-2010_02