HuagongsheHuagongshe Chemistry Print Report · For research reference only
Formaldehyde → Methyl 4-chloro-3-(dimethylamino)benzo[b]thiophene-2-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Methyl 3-amino-4-chloro-1-benzothiophene-2-carboxylate | HCID 2818443 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Water | HCID 962 | — |
| Product | Methyl 4-chloro-3-(dimethylamino)benzo[b]thiophene-2-carboxylate | HCID 18963790 | — |
Reaction Steps
A mixture of methyl 3-amino-4-chlorobenzo[b]thiophene-2-carboxylate (1.7 g, 7.0 mmol) [Beck J. R., supra] and paraformaldehyde (2.0 g, 67 mmol) in 45 mL of acetic acid is treated in portions with sodium cyanoborohydride (2.0 g, 32 mmol). The mixture is stirred at room temperature for 24 hours, then diluted cautiously with 250 g of ice and water. Solid sodium carbonate is added until the mixture is slightly basic. After extraction with ethyl acetate, the combined organic layers are washed with brine, then dried (anhydrous sodium sulfate), and evaporated to provide methyl 4-chloro-3-(dimethylamino)benzo[b]thiophene-2-carboxylate as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05350748 |
| Source dataset | uspto-grants-1994_09 |
| ORD ID | ord-c22f4b6d166f4ad583e4c3b8f6b48483 |
| Source note | uspto-grants-1994_09 |