HuagongsheHuagongshe Chemistry Print Report · For research reference only
Oxalyl chloride → HCID 22719746, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | HCID 22719744 | HCID 22719744 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 22719746 | HCID 22719746 | — |
Reaction Steps
Oxalyl chloride (1.15 ml, 13.2 mmol) was added to an ice-cooled solution of 1-{2-[(benzyloxy)carbonyl]pentyl}cyclopentanecarboxylic acid (EP 274234) (2.0 g, 6.3 mmol) in dry dichloromethane (20 ml), and the solution stirred at room temperature for 2 hours. The reaction mixture was concentrated under reduced pressure and the residue azetroed with dichloromethane (3×), to give the title compound as a golden oil, 2.1 g; 1H NMR (CDCl3, 300 MHz) δ: 0.88 (t, 3H), 1.28 (m, 2H), 1.43 (m, 2H), 1.63 (m, 6H), 2.00 (m, 1H), 2.08-2.35 (m, 3H), 2.44 (m, 1H), 5.15 (s, 2H), 7.28 (m, 5H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06734186B1 |
| Source dataset | uspto-grants-2004_05 |
| ORD ID | ord-13f6d18069d94c9d88fa1b959ef60687 |
| Source note | uspto-grants-2004_05 |