HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → HCID 20098370, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | HCID 20098375 | HCID 20098375 | — |
| Product | HCID 20098370 | HCID 20098370 | — |
Reaction Steps
A suspension of 2.6 g of the product of Step A in 70 ml of tetrahydrofuran was cooled to 0° to 5° C. and then 4.7 ml of acetic anhydride were added. The mixture was held at room temperature for 3 hours and was then evaporated to dryness under reduced pressure at 50° C. The residue was taken up in a 1-1 mixture of chloroform-methanol and was filtered. The product was dried at 80° C. to obtain 2.7 g of 5-acetylamino-2-acetoxy-N-(1H-indol-4-yl)-benzamide melting at 263° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04908367 |
| Source dataset | uspto-grants-1990_03 |
| ORD ID | ord-53b98cc2eea6445585a4beaaffcbf9d3 |
| Source note | uspto-grants-1990_03 |