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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1622964Generated: October 31, 2026

Boron trifluoride etherate → HCID 15534394, compound

https://huagongshe.com/reaction/1622964

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoron trifluoride etherateHCID 8000—
ReactantN-((Benzyloxy)carbonyl)-2-methylalanineHCID 294936—
ReactantSodium BicarbonateHCID 516892—
ReactantTert-butyl 2,2,2-trichloroethanimidateHCID 2734700—
SolventDichloromethaneHCID 6344—
SolventCyclohexaneHCID 8078—
ProductHCID 15534394HCID 1553439470%

Reaction Steps

To a solution of N-[(benzyloxy)carbonyl]-2-methylalanine (1 g, 4.21 mmol) in DCM (10 ml anhydrous), cyclohexane (10 ml) at 0° C. under nitrogen was added boron trifluoride diethyl etherate (7.7 μl, catalytic). tert-Butyl 2,2,2-trichloroacetimidate (1.51 ml, 8.43 mmol) in cyclohexane (10 ml) was then added slowly over 30 minutes before allowing to warm to RT. Reaction was allowed to stir at RT for 16 hours. To the crude reaction mixture was added 190 mg of NaHCO3 and the reaction filtered. The mother liquors were concentrated in vacuo. The crude extract was purified by column chromatography (10% EtOAc in heptane) to yield the desired product (0.863 g, 70% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08778953B2
Source datasetuspto-grants-2014_07
ORD IDord-a45f128fa6d14856924abfead762c2f0
Source noteuspto-grants-2014_07