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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1053576Generated: October 31, 2026

N-Ethylaniline → HCID 71613319, compound

https://huagongshe.com/reaction/1053576

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-EthylanilineHCID 7670—
ReactantDiisopropylethylamineHCID 81531—
Reactant4-(3-Bromopropoxy)phenolHCID 12439900—
SolventAcetonitrileHCID 6342—
ProductHCID 71613319HCID 7161331930%

Reaction Conditions

Temperature70 °C

Reaction Steps

Compound 10a (500 mg, 2.2 mmol) and N-ethylaniline (1 g, 5.5 mmol) were reacted in acetonitrile for 30 mins before diisopropylethylamine (284 mg, 2.2 mmol) was added dropwise. The reaction mixture was then heated and stirred at 70° C. for 12 hours. After cooling to room temperature, the solvent was evaporated and the residue was purified by silica gel column chromatography to provide the compound 10 (170 mg, 0.66 mmol, 24% yield) as a pale yellow solid. MS (ESI, positive) m/z calcd. for C17H21NO2 [M+H]+: 272.16, found: 272.00. 1H NMR (400 MHz, Chloroform-d) δ 7.25 (d, J=7.8 Hz, 2H), 6.88-6.66 (m, 7H), 3.99 (t, J=5.8 Hz, 2H), 3.53 (t, J=7.1 Hz, 2H), 3.41 (q, J=7.2 Hz, 2H), 2.08 (q, J=6.7 Hz, 2H), 1.19 (t, J=7.1 Hz, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09394233B2
Source datasetuspto-grants-2016_07
ORD IDord-9fd6f7463e734d18b47ae74c40cb7e64
Source noteuspto-grants-2016_07