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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 433292Generated: October 29, 2026

HCID 12110002, compound → HCID 12110003, compound

https://huagongshe.com/reaction/433292

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 12110002HCID 12110002—
ReactantHCID 178418287HCID 178418287—
SolventDichloromethaneHCID 6344—
ProductHCID 12110003HCID 1211000371%

Reaction Steps

A mixture of 4-amino-2-[1-(3-ethoxy-4-methoxyphenyl)-3-hydroxybutyl]isoindoline-1,3-dione (0.7 g, 1.82 mmol), pyridinium chlorochromate (0.79 g, 3.64 mmol) and Celite (0.6 g) in methylene chloride (40 mL) was stirred at room temperature for 4 hours. The mixture was filtered through celite and the filtrate was washed with water, brine, dried and concentrated. The residue was purified by chromatography (silica gel, methylene chloride:ethyl acetate 95:5) to give 4-amino-2-[1-(3-ethoxy-4-methoxyphenyl)-3-oxobutyl]isoindoline-1,3-dione as a white solid (0.49 g, 71%); 1H NMR (CDCl3) δ7.38-7.31 (t, J=7.3 Hz, 1H), 7.08-7.05 (m, 3H), 6.81-6.77 (m, 2H), 5.74-5.67 (dd, J=5.9 and 9.4 Hz, 1H), 5.20 (s, 2H), 4.11 (q, J=7.0 Hz, 2H), 3.98-3.87 (dd, J=9.5 and 17.8 Hz, 1H), 3.83 (s, 3H), 3.33-3.23 (dd, J=5.6 and 17.7 Hz, 1H), 2.18-(s, 3H), 1.44 (t, J-6.9 Hz, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06667316B1
Source datasetuspto-grants-2003_12
ORD IDord-930408508caa47b1aef4c8cf039477ab
Source noteuspto-grants-2003_12