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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 551054Generated: November 3, 2026

p-Toluenesulfonic acid monohydrate → HCID 86622848, compound

https://huagongshe.com/reaction/551054

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 numberUS07947677B2
Source datasetuspto-grants-2011_05
ORD IDord-7d4a4c8dca184764b18055abba01ebae
Source noteuspto-grants-2011_05