HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Acetoxybenzoyl chloride → 3-Acetamidobicyclo[1.1.1]pentan-1-yl 2-acetoxybenzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Acetoxybenzoyl chloride | HCID 79668 | — |
| Reactant | N-{3-hydroxybicyclo[1.1.1]pentan-1-yl}acetamide | HCID 86287953 | — |
| Product | 3-Acetamidobicyclo[1.1.1]pentan-1-yl 2-acetoxybenzoate | HCID 86288027 | — |
Reaction Steps
The general procedure of Example 1 Step 3 is repeated starting with N-(3-hydroxybicyclo[1.1.1]pentan-1-yl)acetamide (1) and using O-acetylsalicyloyl chloride in place of the acetyl chloride to produce 3-acetamidobicyclo[1.1.1]pentan-1-yl 2-acetoxybenzoate (8).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09447025B2 |
| Source dataset | uspto-grants-2016_09 |
| ORD ID | ord-273eca5867b241388ceba11b41776f3b |
| Source note | uspto-grants-2016_09 |