HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl chloroformate → Methyl 5-methylthiophene-3-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl chloroformate | HCID 6586 | — |
| Reactant | 4-Bromo-2-methylthiophene | HCID 638584 | — |
| Product | Methyl 5-methylthiophene-3-carboxylate | HCID 4644182 | — |
Reaction Steps
Alternatively, initial lithiation of 3-bromo-5-methylthiophene followed by capture with methyl chloroformate gives methyl 5-methylthiophene-3-carboxylate. Free-radical bromination of the methyl group followed by treatment with an alkali azide, subsequent reduction and hydrolysis provides 5-(aminomethyl)thiophene-3-carboxylic acid (VI). ##STR38##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05849693 |
| Source dataset | uspto-grants-1998_12 |
| ORD ID | ord-dd43a9d7e64b4608953bce55cb6f7edc |
| Source note | uspto-grants-1998_12 |