HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 19972023, compound → HCID 19972018, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 19972023 | HCID 19972023 | — |
| Reactant | HCID 178478979 | HCID 178478979 | — |
| Product | HCID 19972018 | HCID 19972018 | 32% |
Reaction Steps
In analogy to Example 11, the benzyl phosphinate 12 is prepared from the bis-substituted benzyl bromophosphinate 8 and a 2.0N phenylmagnesium chloride solution in a yield of 32%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05608098 |
| Source dataset | uspto-grants-1997_03 |
| ORD ID | ord-8401af28b19b46b1bfd494d817e44d52 |
| Source note | uspto-grants-1997_03 |