HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzene → HCID 15617948, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzene | HCID 241 | — |
| Reactant | Pyrrolidine | HCID 31268 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | HCID 15617944 | HCID 15617944 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 15617948 | HCID 15617948 | 76% |
Reaction Steps
A mixture of -he compound of Example 131 Part B (1.00 g, 3.0 mmole), oxalyl chloride (1.3 mL, 15.0 mmole) and benzene (10 mL) was stirred at room temperature for 21 hours and concentrated under vacuum. The residue was dissolved in methylene chloride (10 mL) and added dropwise to a stirred solution of pyrrolidine (0.53 mL, 6.3 mmole) in methylene chloride (10 mL) at 0°. After 6.5 hours, the mixture was diluted with ether, washed with water and 1.0N hydrochloric acid, then dried over magnesium sulfate and concentrated under vacuum. The crude material was hydrogenated using the procedure of Example 86. Recrystallization of the crude product (ethyl acetate/ethanol) provided the title compound (0.63 g, 76%) as an off-white solid, mp 166°-160°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05026759 |
| Source dataset | uspto-grants-1991_06 |
| ORD ID | ord-f326cbf81a664af5b58ebb75cba32911 |
| Source note | uspto-grants-1991_06 |