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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1696388Generated: November 1, 2026

p-Toluenesulfonic acid monohydrate → HCID 86622848, compound

https://huagongshe.com/reaction/1696388

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acid monohydrateHCID 521998—
ReactantHCID 57426210HCID 57426210—
SolventTolueneHCID 1140—
ProductHCID 86622848HCID 86622848—

Reaction Steps

To a solution of ethyl 3-[4-amino-1-(2-tert-butoxy-2-oxoethyl)-1H-indol-3-yl]propanoate from Step C (1.00 g, 2.89 mmol) in toluene (50 mL) was added p-toluenesulfonic acid monohydrate (5 mg, 0.026 mmol) and the mixture was heated at reflux. After 2 h, the reaction was allowed to cool to ambient temperature and the mixture was washed with saturated aqueous NaHCO3 (10 mL). The organic layer was dried over Na2SO4, filtered, and concentrated in vacuo. The crude product was purified by silica gel chromatography, eluting with a gradient of CH2Cl2:MeOH—100:0 to 92:8, to give the title compound. MS: m/z=301 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08163752B2
Source datasetuspto-grants-2012_04
ORD IDord-9402901d071045b1b50578d8c0ffe3c4
Source noteuspto-grants-2012_04