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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 245937Generated: October 26, 2026

Potassium Carbonate → 2-((R)-1-tert-butoxycarbonylamino-ethyl)-4,5-dihydrooxazole-4-carboxylic acid methyl ester

https://huagongshe.com/reaction/245937

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant(Diethylamino)sulfur trifluorideHCID 123472—
Reactantmethyl 2-((R)-2-(tert-butoxycarbonylamino)propanamido)-3-hydroxypropanoateHCID 57486672—
SolventDichloromethaneHCID 6344—
Product2-((R)-1-tert-butoxycarbonylamino-ethyl)-4,5-dihydrooxazole-4-carboxylic acid methyl esterHCID 7127982195.8%

Reaction Conditions

Temperature-76 °C

Reaction Steps

In a round-bottomed flask, 2-((R)-2-tert-butoxycarbonylamino-propionylamino)-3-hydroxy-propionic acid methyl ester (419 mg, 1.3 mmol) was dissolved in dichloromethane (11 ml). The solution was cooled to −76° C. and DAST (0.20 ml, 1.51 mmol) was added dropwise. The light yellow solution was stirred at −76° C. for 2 h then anhydrous potassium carbonate (269 mg, 1.95 mmol) was added in one portion. The reaction mixture was allowed to warm to room temperature, quenched with 10 ml of saturated aqueous NaHCO3 and extracted with dichloromethane (3×). The organic layers were combined, dried over sodium sulfate, filtered and concentrated to afford 339 mg (91%) of 2-((R)-1-tert-butoxycarbonylamino-ethyl)-4,5-dihydro-oxazole-4-carboxylic acid methyl ester as a brown oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08658646B2
Source datasetuspto-grants-2014_02
ORD IDord-f52634fe79464d7e929a0012ce3f3e1e
Source noteuspto-grants-2014_02