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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1436522Generated: November 3, 2026

Trifluoroacetic acid → HCID 69018507, compound

https://huagongshe.com/reaction/1436522

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantChloromethyl Methyl EtherHCID 7864—
ReactantBoron trifluoride etherateHCID 8000—
Reactant1-Phenethylamine, (-)-HCID 75818—
Reactant2-KetobutyrateHCID 3593277—
Reactant5-(Methoxymethyl)cyclopenta-1,3-dieneHCID 12547288—
ReactantHCID 178507085HCID 178507085—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
ProductHCID 69018507HCID 6901850725%

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07618978B2
Source datasetuspto-grants-2009_11
ORD IDord-c4c69a0d9d3344e087f38984250ab016
Source noteuspto-grants-2009_11