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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1681001Generated: November 2, 2026

HCID 57055398, compound → HCID 57058407, compound

https://huagongshe.com/reaction/1681001

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 57055398HCID 57055398—
CatalystHCID 178418390HCID 178418390—
SolventHydrochloric AcidHCID 313—
SolventEthanolHCID 702—
ProductHCID 57058407HCID 5705840763.3%

Reaction Steps

1.94 g of (2R,3S)-2-benzyloxy-3-butoxybutane was dissolved in a mixture of 80 ml of ethanol and 8 ml of 2 N hydrochloric acid. Thereto was added 200 mg of 5% palladium carbon. The mixture was subjected to hydrogenation at the atmospheric pressure at room temperature. After the completion of the reaction, the catalyst was removed by filtration and the filtrate was subjected to distillation. The residue was diluted with water and extracted with dichloromethane three times. The extract was dried and concentrated. The residue was subjected to Kugel-rohr distillation (30 mmHg) to obtain 0.76 g of (2R,3S)-3-butoxy-2-butanol. The 1H-NMR and IR spectrum of this compound were completely agreed with those of (2S,3R)-3-butoxy-2-butanol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05167863
Source datasetuspto-grants-1992_12
ORD IDord-52580015ad07444d8aa01495fe85f965
Source noteuspto-grants-1992_12