HuagongsheHuagongshe Chemistry Print Report · For research reference only
Oxalyl chloride → HCID 20063329, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | HCID 19778163 | HCID 19778163 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 20063329 | HCID 20063329 | — |
Reaction Steps
A solution of (E)-3-[4-(4-fluorophenyl)-2-isopropyl-1-oxo-1,2-dihydroisoquinolin-3-yl]prop-2-enoic acid (0.35 g) in dry tetrahydrofuran (10 ml) was treated with oxalyl chloride (0.26 ml) and heated at reflux for 2 hours. The solvent was then removed by distillation and the residual yellow solid was washed with petroleum ether (b.p. 40°-60° C.), to give (E)-3-[4-(4-fluorophenyl)-2-isopropyl-1-oxo-1,2-dihydroisoquinolin-3-yl]prop-2-enoyl chloride in the form of a pale yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05004747 |
| Source dataset | uspto-grants-1991_04 |
| ORD ID | ord-7389806d9221485b82aa504164296330 |
| Source note | uspto-grants-1991_04 |