HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-(Bromoacetyl)benzonitrile → HCID 70224701, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-(Bromoacetyl)benzonitrile | HCID 98654 | — |
| Reactant | Potassium bis(trimethylsilyl)amide | HCID 3251421 | — |
| Reactant | HCID 88219294 | HCID 88219294 | — |
| Product | HCID 70224701 | HCID 70224701 | — |
Reaction Steps
Using the same procedure as described in Example 2C, the reaction of the title compound of 30A (10.3 mmol) and 4-cyanophenacyl bromide (11.3 mmol) in the presence of potassium bis(trimethylsilyl)amide (11.3 mmol) generated the title compound of 30B, 4.82 g (8.4 mmol, 84% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06194438B1 |
| Source dataset | uspto-grants-2001_02 |
| ORD ID | ord-c25e553ca43b449fbaa3035d3509fd60 |
| Source note | uspto-grants-2001_02 |