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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 348869Generated: October 26, 2026

Potassium Carbonate → tert-Butyl 3-(benzyloxy)-1-(hydroxymethyl)propylcarbamate

https://huagongshe.com/reaction/348869

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantSodium borohydrideHCID 4311764—
Reactantmethyl O-benzyl-N-(tert-butoxycarbonyl)homoserinateHCID 54564501—
SolventEthanolHCID 702—
Producttert-Butyl 3-(benzyloxy)-1-(hydroxymethyl)propylcarbamateHCID 21087273—

Reaction Steps

To an ice-cold solution of methyl O-benzyl-N-(tert-butoxycarbonyl)homoserinate (6 g, 18.6 mmol) in absolute ethanol (100 mL) is added sodium borohydride (2.8 g, 74.2 mmol), and the reaction is refluxed 2 h. The solution is cooled, excess saturated potassium carbonate added, and stirred 16 h at room temperature. The ethanol is removed under reduced pressure, and the aqueous solution is extracted with chloroform. The organic layer is washed with saturated sodium bicarbonate, saturated sodium sulfate, dried (magnesium sulfate), filtered, and concentrated under reduced pressure to give the title compound. ESI MS m/z 296.2 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07176242B2
Source datasetuspto-grants-2007_02
ORD IDord-99f8aeb9ce2e4da2bad8e2d891cc85b8
Source noteuspto-grants-2007_02