HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl (3E)-4-phenyl-3-butenoate → (3E)-4-Phenyl-3-buten-1-ol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl (3E)-4-phenyl-3-butenoate | HCID 5370649 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (3E)-4-Phenyl-3-buten-1-ol | HCID 5370624 | — |
Reaction Steps
In an analogous manner to that described in Example 5 (b), by reducing methyl (E)-4-phenyl-but-3-enoate by means of lithium aluminium hydride in tetrahydrofuran there was obtained (E)-4-phenyl-but-3-en-1-ol, which was converted into (E)-4-phenyl-but-3-enyl methanesulphonate in analogy to the procedure described in J.Chem.Soc. Perk.Trans. 1 (1988), (6), 1517-1519 for the preparation of the (Z) isomer.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06051712 |
| Source dataset | uspto-grants-2000_04 |
| ORD ID | ord-16a348a886454436a10a87b2cb79139a |
| Source note | uspto-grants-2000_04 |