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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1651862Generated: October 31, 2026

4-Toluenesulfonyl chloride → Methyl 4-(2-p-toluenesulphonamido-indan-5-yl)-4-oxobutyrate

https://huagongshe.com/reaction/1651862

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Toluenesulfonyl chlorideHCID 7397—
ReactantTriethylamineHCID 8471—
ReactantMethyl 4-(2-amino-indan-5-yl)-4-oxobutyrate hydrochlorideHCID 23050575—
SolventChloroformHCID 6212—
ProductMethyl 4-(2-p-toluenesulphonamido-indan-5-yl)-4-oxobutyrateHCID 14071511—

Reaction Steps

6.0 g (21.1 mmol) of methyl 4-(2-amino-indan-5-yl)-4-oxobutyrate hydrochloride are suspended in 60 ml of chloroform and 5.0 g (25.3 mmol) of p-toluenesulphonyl chloride are added. 5.1 g (50 mmol) of triethylamine are added, with vigorous stirring, a clear solution being formed. After 20 hours at room temperature, the mixture is washed with water, the chloroform solution is evaporated and the residue is recrystallised from methanol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04929754
Source datasetuspto-grants-1990_05
ORD IDord-bc74755d74a348fcb590a473b933705a
Source noteuspto-grants-1990_05