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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1627031Generated: October 31, 2026

Boron trifluoride etherate → HCID 86701295, compound

https://huagongshe.com/reaction/1627031

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoron trifluoride etherateHCID 8000—
Reactant154632-86-7HCID 4255958—
ReactantHCID 86701294HCID 86701294—
SolventChloroformHCID 6212—
ProductHCID 86701295HCID 8670129535%
ProductHCID 86701296HCID 8670129617%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of (2S,3S,4S)-2,3-bis(2-methylallyloxy)pentane-1,4-diol (920 milligrams (mg), 3.77 mmol) and (S)-1-benzyl 2-methyl aziridine-1,2-dicarboxylate (0.739 mL, 3.74 mmol) in anhydrous chloroform (CHCl3; 5 mL) was added BF3-Et2O (26 microliters (μL) 0.55 mmol) at 0° C. and the solution was stirred at 0° C. for 3 h. The crude reaction mixture was concentrated and purified by flash chromatography (SiO2) to furnish (S)-methyl 2-(benzyloxycarbonylamino)-3-((2S,3S,4S)-4-hydroxy-2,3-bis(2-methylallyloxy)-pentyloxy)-propanoate as a colorless oil (620 mg, 35%) and (S)-methyl 2-(benzyloxycarbonylamino)-3-((2S,3S,4S)-5-hydroxy-3,4-bis(2-methylallyloxy)pentan-2-yloxy)propanoate as a colorless oil (300 mg, 17%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08785479B2
Source datasetuspto-grants-2014_07
ORD IDord-2eaeadbb4f4d4ed089970d584cd73351
Source noteuspto-grants-2014_07