Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | 2-Cyclopentyl-5,6,7,8-tetrahydro-indolizine | HCID 66851048 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 86649693 | HCID 86649693 | 88% |
Reaction Steps
2-Cyclopentyl-5,6,7,8-tetrahydro-indolizine (0.24 g, 1.27 mmol) was dissolved in THF (1 mL) and toluene (1.5 mL) and cooled to 0° C. Oxalyl chloride (0.14 mL, 1.52 mmol) was added dropwise and the mixture was stirred at 0° C. for 30 min, then at room temperature for 1 hour. Concentration in vacuo afforded (2-cyclopentyl-5,6,7,8-tetrahydro-indolizin-3-yl)-oxo-acetyl chloride (0.31 g, 88%) as a semi-solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08524705B2 |
|---|
| Source dataset | uspto-grants-2013_09 |
|---|
| ORD ID | ord-d0991700f12c494e97606c7c2657724e |
|---|
| Source note | uspto-grants-2013_09 |
|---|