HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2282997Generated: October 31, 2026
Boron trifluoride etherate → HCID 86701295, compound
https://huagongshe.com/reaction/2282997
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Boron trifluoride etherate | HCID 8000 | — |
| Reactant | 154632-86-7 | HCID 4255958 | — |
| Reactant | HCID 86701294 | HCID 86701294 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 86701295 | HCID 86701295 | 35% |
| Product | HCID 86701296 | HCID 86701296 | 17% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09144239B2 |
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| Source dataset | uspto-grants-2015_09 |
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| ORD ID | ord-820c6c81d4954a518cba2316ebb81055 |
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| Source note | uspto-grants-2015_09 |
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