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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2222959Generated: October 31, 2026

Water → HCID 68800773, compound

https://huagongshe.com/reaction/2222959

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantEthyl orthoformateHCID 31214—
ReactantDi-tert-butyl dicarbonateHCID 90495—
ReactantHCID 18540457HCID 18540457—
SolventTolueneHCID 1140—
SolventSodium chloride; waterHCID 57417360—
ProductHCID 68800773HCID 6880077359%

Reaction Conditions

Temperature75 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07371869B2
Source datasetuspto-grants-2008_05
ORD IDord-1162309c5e83443f935224cf01d5890d
Source noteuspto-grants-2008_05