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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 864845Generated: October 25, 2026

Trifluoroacetic acid → Ethyl 6-[4-(4-pyridylamino)phenoxy]hexanoate

https://huagongshe.com/reaction/864845

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
Reactantethyl 6-[4-[N-(4-pyridyl)-N-tertiary-butyloxycarbonylamino]phenoxy]hexanoateHCID 18918347—
SolventDichloromethaneHCID 6344—
ProductEthyl 6-[4-(4-pyridylamino)phenoxy]hexanoateHCID 18918592—

Reaction Steps

Trifluoroacetic acid (3 ml) was added to a stirred solution of ethyl 6-[4-[N-(4-pyridyl)-N-tertiary-butyloxycarbonylamino]phenoxy]hexanoate (260 mg) dissolved in dichloromethane (3 ml). After 18 hours the solvents were removed in vacuo and the residual gum dissolved in dichloromethane. This solution was treated with a saturated solution of sodium hydrogen carbonate. The organic phase was washed with water, dried and evaporated. Trituration of the residue with hexane gave the title compound, 120 mg, as a white solid: m.p. 104°-106° C.; NMR (CDCl3) δ8.22 (2H, d), 7.12 (2H, d), 6.90 (2H, d), 6.64 (.2H, dd), 5.82 (1H, s), 4.13 (2H, q), 3.97 (2H, t), 2.34 (2H, t), 1.80 (2H, m), 1.70 (2H, m), 1.53 (2H, m), 1.27 (3H, t); m/e 329 (M+H)+ ; calculated for C19H24N2O3.0.25H2O: C, 68.6; H, 7.4; N, 8.4. found: C, 68.8; H, 7.3; N, 8.2%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05563141
Source datasetuspto-grants-1996_10
ORD IDord-fa616cee9d3745b9839d3048beee2077
Source noteuspto-grants-1996_10