HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → HCID 19882593, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | HCID 19098380 | HCID 19098380 | — |
| Product | HCID 19882593 | HCID 19882593 | — |
Reaction Steps
The product from Example 14 was treated with KOH to give the free base, then reacted with acetic anhydride affording the amide. Anal. calcd. for C14H19NO2 : C, 72.07; H, 8.21; N, 6.00. Found: C, 72.03; H, 8.25; N, 6.01. This amide was reduced using the procedure of Example 5 to give the desired compound. Anal. calcd. for C14H22ClNO: C, 65.74; H, 8.67; N, 5.48. Found: C, 65.71; H, 8.61; N, 5.47.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05140040 |
| Source dataset | uspto-grants-1992_08 |
| ORD ID | ord-f425a93e3e5f45ea973777908715f94c |
| Source note | uspto-grants-1992_08 |