HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → Methyl 6-nitro-1-benzothiophene-2-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methyl Thioglycolate | HCID 16907 | — |
| Reactant | 2,4-Dinitrobenzaldehyde | HCID 68250 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | Methyl 6-nitro-1-benzothiophene-2-carboxylate | HCID 23626901 | — |
Reaction Steps
24.8 g (126.7 mmol) of 2,4-dinitrobenzaldehyde, 13.4 g (126.7 mmol) of methyl mercaptoacetate and 35.3 ml (253.3 mmol) of triethylamine in 74.5 ml of DMSO are heated at 80° C. for 1 h. The reaction solution is poured into 250 ml of ice-water. The resulting precipitate is filtered off with suction, washed with water and dried at 50° C. under reduced pressure overnight. This gives 16.1 g (53.6% of theory) of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08884017B2 |
| Source dataset | uspto-grants-2014_11 |
| ORD ID | ord-563afe14a26241388e4aceaf43954582 |
| Source note | uspto-grants-2014_11 |