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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1695020Generated: November 1, 2026

(4S,5S)-4-[(Benzyloxy)methyl]-5-(iodomethyl)-2,2-dimethyl-1,3-dioxolane → (2R)-1-(benzyloxy)but-3-en-2-ol

https://huagongshe.com/reaction/1695020

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(4S,5S)-4-[(Benzyloxy)methyl]-5-(iodomethyl)-2,2-dimethyl-1,3-dioxolaneHCID 66645664—
CatalystZincHCID 23994—
SolventEthanolHCID 702—
Product(2R)-1-(benzyloxy)but-3-en-2-olHCID 9989803100.3%

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of 49.20 g of the crude (4S,5S)-4-[(benzyloxy)methyl]-5-(iodomethyl)-2,2-dimethyl-1,3-dioxolane obtained in Reference Example (1c) (136 mmol) and 26.66 g of zinc powder (408 mmol) in ethanol (420 ml) was stirred at 80° C. for three hours. After cooling the reaction mixture, the unreacted zinc powder was separated by filtration using Celite 545 and washed with ethanol. The filtrate was concentrated under reduced pressure and diluted with 1 M hydrochloric acid, followed by extraction with ethyl acetate. Then, the organic layer was washed with water, a 1.5 M sodium sulfite aqueous solution and brine and dried over anhydrous magnesium sulfate. After filtration, the solvent was evaporated under reduced pressure to obtain 24.29 g of the crude title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08158790B2
Source datasetuspto-grants-2012_04
ORD IDord-f89adf3a876a4cd6b89d681d261aea14
Source noteuspto-grants-2012_04