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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 891215Generated: October 30, 2026

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

https://huagongshe.com/reaction/891215

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 numberUS07001899B2
Source datasetuspto-grants-2006_02
ORD IDord-3f60a1ecbef64dee8d10143acfbb30e3
Source noteuspto-grants-2006_02