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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 393874Generated: October 29, 2026

3-(Dimethylamino)phenol → 3-Dimethylaminophenyl 5-[(1,2-dihydro-1,2-dioxonaphth-4-yl)oxy]valerate

https://huagongshe.com/reaction/393874

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(Dimethylamino)phenolHCID 7421—
ReactantDicyclohexylcarbodiimideHCID 10868—
Reactant5-[(1,2-Dioxo-1,2-dihydronaphth-4-yl)oxy]valeric AcidHCID 22647822—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventTetrahydrofuranHCID 8028—
Product3-Dimethylaminophenyl 5-[(1,2-dihydro-1,2-dioxonaphth-4-yl)oxy]valerateHCID 980071936%

Reaction Steps

A mixture of acid 3 (137 mg, 0.5 mmol), 3-dimethylaminophenol (82 mg, 0.6 mmol), DCC (103 mg, 0.5 mmol), and DMAP (12 mg, 0.01 mmol) in THF (2 mL) was stirred for 2 h. The reaction mixture was concentrated in vacuo, the residue dissolved in benzene, washed with H2O and dried (Na2SO4). Column chromatography (10% EtOAc) in benzene gave 13 as a yellow solid (70 mg, 36%), 1H NMR (CDCl3) 8.13, (d, J=7.3 Hz, 1H), 7.90 (d, J=7.4 Hz, 1H), 7.69 (t, J=6.1 Hz, 1H), 7.58 (t, J=7.6 Hz, 1H), 7.22 (dd, J=8.1, 8.1 Hz, 1H), 6.30-6.70 (m, 2H), 5.96 (s, 1H), 4.21 (t, J=5.6 Hz, 2H), 2.69 (t, J=6.5 Hz, 2H), 1.90-2.15 (m, 4H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06809176B2
Source datasetuspto-grants-2004_10
ORD IDord-cd1d138584874f81ac76ac8bb285d186
Source noteuspto-grants-2004_10