HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methoxymethyl-triphenylphosphonium chloride → HCID 178444484, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methoxymethyl-triphenylphosphonium chloride | HCID 2723798 | — |
| Reactant | HCID 178444538 | HCID 178444538 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 178444484 | HCID 178444484 | — |
Reaction Steps
In a manner analogous to that described in Example 2, paragraphs (a) and (b), trans-4-pentylcyclohexanecarboxaldehyde was reacted in a Wittig reaction with methoxymethyl-triphenylphosphonium chloride and potassium t-butylate and the resulting enol ether was subsequently hydrolyzed in tetrahydrofuran/2N hydrochloric acid to give (trans-4-pentylcyclohexyl)acetaldehyde.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04630896 |
| Source dataset | uspto-grants-1986_12 |
| ORD ID | ord-8ccbb91307b545b69bccb48e8ca5532c |
| Source note | uspto-grants-1986_12 |