HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 862939Generated: October 28, 2026
Oxalyl chloride → HCID 18703878, compound
https://huagongshe.com/reaction/862939
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | HCID 21714793 | HCID 21714793 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 18703878 | HCID 18703878 | 94% |
Reaction Steps
To ice-cold DMF (1 ml) under an argon atmosphere was added oxalyl chloride (68 ml, 0.78 mmol). After stirring for 5 min at 0° C., a solution of (1RS,2SR,3SR)-1-(4-methoxyphenyl)-3-(3,4-methylenedioxyphenyl)indane2-carboxamide (150 mg, 0.39 mmol) in DMF (2 ml) was added, and stirring was continued for an additional 10 min at 0° C. The reaction mixture was partitioned between EtOAc and 3M HCl. The aqueous phase was extracted with EtOAc, and the combined organic extracts were washed successively with H2O, aqueous NaHCO3, H2O and saturated aqueous NaCl and dried. The solvent was removed in vacuo to afford the title compound as a white solid (135 mg, 94%) which was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05719182 |
|---|
| Source dataset | uspto-grants-1998_02 |
|---|
| ORD ID | ord-9320fa3ccb3e41c4b8476dc28fc62091 |
|---|
| Source note | uspto-grants-1998_02 |
|---|