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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 722738Generated: October 31, 2026

p-Toluenesulfonic acid → 3-Allyloxycarbonylamino-4,4-diethoxy-butyric acid tert-butyl ester

https://huagongshe.com/reaction/722738

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acidHCID 6101—
Reactant3-Allyloxycarbonylamino-4-oxo-butyric acid tert-butyl esterHCID 18465715—
ReactantEthylorthoformateHCID 53630039—
SolventEthanolHCID 702—
Product3-Allyloxycarbonylamino-4,4-diethoxy-butyric acid tert-butyl esterHCID 23598712—

Reaction Steps

To a solution of 3-allyloxycarbonylamino-4-oxo-butyric acid tert-butyl ester, 102, (13.3 g, 51.7 mmol) in anhydrous ethanol (75 mL) is added ethyl orthoformate (45 mL, 0.270 mol), p-toluenesulfonic acid (0.15 g, cat.) and 4 Å molecular sieves (10 g, kiln dried) under N2. After the consumption of starting material, the sieves are removed by filtration and the solvent removed in vacuo to provide the desired compound as a clear oil which is used directly without further purification. MS (ESI): m/e=332.21 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07138395B2
Source datasetuspto-grants-2006_11
ORD IDord-d3c7151eb2394f10b5d061509ecc4bc5
Source noteuspto-grants-2006_11