HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1436522Generated: November 3, 2026
Trifluoroacetic acid → HCID 69018507, compound
https://huagongshe.com/reaction/1436522
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Chloromethyl Methyl Ether | HCID 7864 | — |
| Reactant | Boron trifluoride etherate | HCID 8000 | — |
| Reactant | 1-Phenethylamine, (-)- | HCID 75818 | — |
| Reactant | 2-Ketobutyrate | HCID 3593277 | — |
| Reactant | 5-(Methoxymethyl)cyclopenta-1,3-diene | HCID 12547288 | — |
| Reactant | HCID 178507085 | HCID 178507085 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 69018507 | HCID 69018507 | 25% |
Reaction Steps
Add molecular sieves (3 Å, 12.0 g), (S)-(−)-α-methylbenzylamine (6.4 mL, 50.0 mmol) to a solution of ethylglyoxalate (10.3 mL, 50.0 mmol) in dichloromethane (200 mL) cooled in an ice bath. Stir the mixture at 0° C. for 2 h, and then cool to −78° C. Add trifluoroacetic acid (4.10 mL, 55.0 mmol), boron trifluoride etherate (6.90 mL, 55.0 mmol), and 5-methoxymethyl-1,3-cyclopentadiene (60.0 mmol, prepared in situ by adding cyclopentadienylsodium (2.0 M in THF, 30.0 mL, 60.0 mmol) to a solution of chloromethyl methyl ether (5.70 mL, 75.0 mmol) in tetrahydrofuran (30 mL) at −55° C.) with a 5 min interval between each addition. Stir for 2 h at −78° C. and refrigerate (−20° C.) overnight. Quench the reaction with saturated aqueous sodium bicarbonate solution (200 mL) and stir the mixture vigorously for 15 min. Separate the layers, dry the organic layer (magnesium sulfate), concentrate, and purify (silica gel chromatography 10:90 to 30:70 ethyl acetate:hexanes) to give the title compound (3.95 g, 25%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07618978B2 |
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| Source dataset | uspto-grants-2009_11 |
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| ORD ID | ord-c4c69a0d9d3344e087f38984250ab016 |
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| Source note | uspto-grants-2009_11 |
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