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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1005159Generated: October 31, 2026

Methyl (3E)-4-phenyl-3-butenoate → (3E)-4-Phenyl-3-buten-1-ol

https://huagongshe.com/reaction/1005159

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl (3E)-4-phenyl-3-butenoateHCID 5370649—
ReactantAluminium lithium hydrideHCID 21226445—
SolventTetrahydrofuranHCID 8028—
Product(3E)-4-Phenyl-3-buten-1-olHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06051712
Source datasetuspto-grants-2000_04
ORD IDord-16a348a886454436a10a87b2cb79139a
Source noteuspto-grants-2000_04