HuagongsheHuagongshe Chemistry Print Report · For research reference only
p-Toluenesulfonic acid → 3-Allyloxycarbonylamino-4,4-diethoxy-butyric acid tert-butyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | 3-Allyloxycarbonylamino-4-oxo-butyric acid tert-butyl ester | HCID 18465715 | — |
| Reactant | Ethylorthoformate | HCID 53630039 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 3-Allyloxycarbonylamino-4,4-diethoxy-butyric acid tert-butyl ester | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07001899B2 |
| Source dataset | uspto-grants-2006_02 |
| ORD ID | ord-3f60a1ecbef64dee8d10143acfbb30e3 |
| Source note | uspto-grants-2006_02 |