HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → Tert.-butyl 2-[(5-bromo-thiophen-2-yl)-carbonylamino]-isobutyrate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 5-Bromothiophene-2-carboxylic acid | HCID 349115 | — |
| Reactant | Tert-butyl 2-amino-2-methylpropanoate hydrochloride | HCID 12186776 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Tert.-butyl 2-[(5-bromo-thiophen-2-yl)-carbonylamino]-isobutyrate | HCID 68638345 | — |
Reaction Steps
2.63 g (12.3 mmol) 5-bromo-thiophene-2-carboxylic acid are refluxed in 15 ml dichloromethane together with 7.0 ml of thionyl chloride for 2 h with stirring. The mixture is then evaporated down i. vac. and the residue is twice taken up in toluene and evaporated down completely i. vac. The residue is added dropwise to 10 ml dichloromethane with stirring at ambient temperature in a mixture of 2.41 g (12.3 mmol) tert.-butyl 2-amino-isobutyrate hydrochloride in 20 ml dichloromethane with 5.14 ml (36.9 mmol) TEA and stirred for 16 h. The mixture is poured into water and extracted with dichloromethane, the combined organic phases are dried over magnesium sulphate and evaporated down i. vac.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07732466B2 |
| Source dataset | uspto-grants-2010_06 |
| ORD ID | ord-85ce16b4205a42c8bd3450e8ff110de5 |
| Source note | uspto-grants-2010_06 |