Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Ethyl orthoformate | HCID 31214 | — |
| Reactant | Di-tert-butyl dicarbonate | HCID 90495 | — |
| Reactant | HCID 18540457 | HCID 18540457 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Sodium chloride; water | HCID 57417360 | — |
| Product | HCID 68800773 | HCID 68800773 | 59% |
Reaction Steps
To a solution of crude 3-(3-amino-4-hydroxy-phenyl)-2-tert-butoxycarbonylamino-propionic acid ethyl ester (0.89 g, 2.74 mmol) in toluene (20 mL) was added triethyl orthoformate (0.57 mL, 3.36 mmol) and the mixture was heated to 75° C. under an atmosphere of argon for 3 hours at which time all starting material had been consumed. The reaction mixture was concentrated in vacuo to a black waxy solid which was dissolved in acetonitrile (25 mL) and di-tert-butyldicarbonate (0.80 g, 3.67 mmol) added. The mixture was stired at ambient temperature under an atmosphere of argon for 16 hours then poured into water (100 mL), diluted with brine (50 mL) and extracted with ethyl acetae (3×50 mL). The combined organic extracts were washed with brine (100 mL), dried over sodium sulfate and concentrated in vacuo to a black viscous oil. Purification by chromatography over silica gel eluted with 35% ethyl acetate/65% hexanes gave (S)-3-benzooxazol-5-yl-2-tert-butoxycarbonylamino-propionic acid ethyl ester as a colorless solid (0.54 g, 59%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07371869B2 |
|---|
| Source dataset | uspto-grants-2008_05 |
|---|
| ORD ID | ord-1162309c5e83443f935224cf01d5890d |
|---|
| Source note | uspto-grants-2008_05 |
|---|