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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 499699Generated: October 30, 2026

HCID 68653695, compound → HCID 68653245, compound

https://huagongshe.com/reaction/499699

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 68653695HCID 68653695—
CatalystPalladiumHCID 23938—
SolventEthyl AcetateHCID 8857—
ProductHCID 68653245HCID 68653245—

Reaction Steps

A mixture of 9.48 g of 4(S)-(2-benzyloxycarbonyl-2-methyl-propyl)-2,2-dimethyl-oxazolidine-3-carboxylic acid tert-butyl ester and 2.58 g of 10% Pd/C in 100 ml of ethyl acetate is hydrogenated at room temperature for 4.5 hours. The solid is removed by filtration over Hyflo®. The mixture is concentrated and re-dissolved in ethyl acetate and 2N NaOH. The layers are separated and the aqueous layer is extracted with ethyl acetate (2×). The aqueous layer is acidified to pH 3 with 4M HCl and extracted with ethyl acetate (3×). The combined organic layers from the second extraction are dried over sodium sulphate, filtered and concentrated. The crude title compound is obtained as a colourless oil. Rf=0.43 (EtOAc-heptane 1:1); Rt=4.23 (gradient I).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07767690B2
Source datasetuspto-grants-2010_08
ORD IDord-cd8d40a739064b009d8afde675996fc0
Source noteuspto-grants-2010_08