HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phenylacetyl chloride → Acetamide, N-(2-(5-methoxyindan-6-yl)ethyl)-2-phenyl-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phenylacetyl chloride | HCID 7679 | — |
| Reactant | Potassium Bicarbonate | HCID 516893 | — |
| Reactant | HCID 12426123 | HCID 12426123 | — |
| Product | Acetamide, N-(2-(5-methoxyindan-6-yl)ethyl)-2-phenyl- | HCID 49798 | — |
Reaction Steps
Using the procedure of Example 1, but with potassium bicarbonate replacing triethylamine, phenylacetyl chloride was reacted with 5-aminoethyl-6-methoxyindan to produce the desired product. After recrystallization from ether it had a melting point of 135° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04232014 |
| Source dataset | uspto-grants-1980_11 |
| ORD ID | ord-fcfcb7d0f5ae4c35ad789873ec611082 |
| Source note | uspto-grants-1980_11 |