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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 634537Generated: October 29, 2026

Diethyl Malonate → Ethyl 3-aminobenzo[b]thiophene-2-carboxylate

https://huagongshe.com/reaction/634537

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl MalonateHCID 7761—
Reactant3-Chloro-1,2-benzisothiazoleHCID 598190—
ReactantSodium ethoxideHCID 2723922—
SolventEthanolHCID 702—
ProductEthyl 3-aminobenzo[b]thiophene-2-carboxylateHCID 73151076.2%

Reaction Steps

A dry 2-neck 500 mL round-bottom flask (RBF) was charged with sodium ethanolate (46.2 mL, 124 mmol), diluted with 151 mL absolute EtOH, cooled in an ice bath and treated dropwise with diethyl malonate (17.98 mL, 118 mmol) under an atmosphere of nitrogen. After stirring for 20 minutes, the ice bath was removed and 3-chlorobenzo[d]isothiazole (20.0 g, 118 mmol) was added in one portion and stirred for 24 hours. The reaction solution was quenched with water, extracted with ether and treated with excess 4 M HCl/dioxane. A pinkish-white precipitate was filtered off, suspended in water, basified with Na2CO3, extracted with ether, washed with water and brine, dried over sodium sulfate, filtered and concentrated to yellow solids (˜20 g) which were recrystallized from ethanol/water and dried in a vacuum oven at 60° C. for 3 hrs to give ethyl 3-aminobenzo[b]thiophene-2-carboxylate (19.9 g, 76% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09324949B2
Source datasetuspto-grants-2016_04
ORD IDord-d15ef6f216d54888a47de35916f4b2c4
Source noteuspto-grants-2016_04