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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 55923Generated: October 25, 2026

Potassium Hydroxide → N-(5-carboxypentyl)-3-(1-naphthoyl)-1H-indole

https://huagongshe.com/reaction/55923

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium HydroxideHCID 14797—
ReactantN-(5-Ethoxycarbonylpentyl)-3-(1-naphthoyl)-1H-indoleHCID 68159362—
SolventOxolane--water (1/1)HCID 21881883—
ProductN-(5-carboxypentyl)-3-(1-naphthoyl)-1H-indoleHCID 68159208—

Reaction Conditions

Temperature60 °C

Reaction Steps

To a solution of 2 (5.0 g, 12 mmol) in a mixture of THF/H2O (1:1) was added potassium hydroxide (1.7 g) and the mixture was stirred at 60° C. for 1 h. The THF was removed under vacuum, the aqueous solution acidified to pH 1 by the addition of hydrochloric acid solution (1N) and extracted by ethyl acetate (3×100 ml). The combined organic phases were washed by water (100 ml), brine solution (100 ml), dried over sodium sulphate, filtered and concentrated to dryness. The crude product obtained was dissolved in ethyl acetate (10 ml) and the Hapten-A precipitated by the addition of a mixture of ether/hexane as a white solid, filtered and dried under high vacuum to give Hapten-A (3.6 g, 78%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09434687B2
Source datasetuspto-grants-2016_09
ORD IDord-17e8838374e3476c959697b133c82e3a
Source noteuspto-grants-2016_09