HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → Ethyl 3-methyl-5-(phenoxycarbonylamino)thiophene-2-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Phenyl chloroformate | HCID 15891 | — |
| Reactant | 5-Amino-3-methylthiophene-2-carboxylate | HCID 86645288 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Ethyl 3-methyl-5-(phenoxycarbonylamino)thiophene-2-carboxylate | HCID 43403943 | 96% |
Reaction Steps
To a stirred mixture of 5-amino-3-methylthiophene-2-carboxylate (11.87 g, 64.08 mmol) and pyridine (5.70 mL, 70.48 mml) in dichloromethane (140 mL) at 0° C. was added dropwise phenyl chloroformate (8.90 mL, 70.71 mmol). The resulting reaction mixture was stirred at ambient temperature for 30 minutes, and then quenched with water (200 mL). The aqueous layer was extracted with dichloromethane (2×200 mL), and the combined organic layer was dried over sodium sulfate, filtered and concentrated in vacuo. The residue was triturated with dichloromethane in hexanes to afford ethyl 3-methyl-5-(phenoxycarbonylamino)thiophene-2-carboxylate as a colorless solid (18.89 g, 96%): MS (ES+) m/z 306.1 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08063084B2 |
| Source dataset | uspto-grants-2011_11 |
| ORD ID | ord-6df8a461fd9749b2acf2f8a0b5939cae |
| Source note | uspto-grants-2011_11 |