Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 570294Generated: October 30, 2026

(Phenylmethoxy)acetaldehyde → 1-(Benzyloxy)pent-4-en-2-ol

https://huagongshe.com/reaction/570294

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(Phenylmethoxy)acetaldehydeHCID 108989—
ReactantHCID 178418473HCID 178418473—
SolventTetrahydrofuranHCID 8028—
Product1-(Benzyloxy)pent-4-en-2-olHCID 10035478—

Reaction Conditions

Temperature0 °C

Reaction Steps

2-(Benzyloxy)acetaldehyde (5 g, 33.3 mmol) in dry THF (10 mL) was added dropwise to a stirred and cooled solution of allylmagnesium chloride (25 mL, 2 M in THF, 50 mmol) in THF (100 mL) at −78° C. After the addition, the solution was allowed to warm to 0° C. and quenched with saturated NH4Cl solution. After standard aqueous work up, the residue was purified over silica using EtOAc and hexane to give 1-(benzyloxy)pent-4-en-2-ol (11).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09023839B2
Source datasetuspto-grants-2015_05
ORD IDord-2ecd7da9568442ffabf69095bebf3b14
Source noteuspto-grants-2015_05