HuagongsheHuagongshe Chemistry Print Report · For research reference only
Chloroform → HCID 67550799, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Chloroform | HCID 6212 | — |
| Reactant | Chlorosuccinimide | HCID 31398 | — |
| Reactant | ethyl 6H-thieno[2,3-b]pyrrole-5-carboxylate | HCID 11708220 | — |
| Solvent | Acetic acid 10-acetoxymethyl-anthracen-9-ylmethyl ester | HCID 613145 | — |
| Product | HCID 67550799 | HCID 67550799 | 74% |
Reaction Steps
To a 0° C. solution of 6H-thieno[2,3-b]pyrrole-5carboxylic acid ethyl ester (180 mg, 0.92 mmol) in acetic add (2 mL) and CHCl3 (2 mL) was added N-chlorosuccinimide (294 mg, 2.2 mmol) over 30 min. The reaction mixture was slowly allowed to warm to room temperature over several hours, stirred overnight, concentrated to remove the chloroform, diluted with water, basified with 5 N NaOH, and extracted with ethyl acetate. The combined organic phases were washed with saturated aqueous NaHCO3, dried over MgSO4, and concentrated. The product was purified by Chromatron-chromatography (4:1 hexanes:ether) and obtained as a white solid (180 mg, 74%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06399601B1 |
| Source dataset | uspto-grants-2002_06 |
| ORD ID | ord-70cd8937d80e4cf2b810523e177930a1 |
| Source note | uspto-grants-2002_06 |