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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diethyl Malonate | HCID 7761 | — |
| Reactant | 3-Chloro-1,2-benzisothiazole | HCID 598190 | — |
| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Ethyl 3-aminobenzo[b]thiophene-2-carboxylate | HCID 731510 | 76.2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09324949B2 |
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| Source dataset | uspto-grants-2016_04 |
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| ORD ID | ord-d15ef6f216d54888a47de35916f4b2c4 |
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| Source note | uspto-grants-2016_04 |
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