Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrafluorophthalic anhydride | HCID 69545 | — |
| Reactant | 1-Phenethylamine, (-)- | HCID 75818 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 182690-76-2 | HCID 9883659 | 74.4% |
Reaction Steps
220 mg of tetrafluorophthalic anhydride and 121 mg of (S)-α-methylbenzylamine were charged in an egg-plant type flask of 50 ml, followed by stirring under heating at a temperature of 180° C. for 2 hours. After cooled, the reaction product was dissolved in chloroform, purified by silica gel column chromatography (eluent; methylene chloride:methanol=30:1 v/v), recrystallized from a mixed solvent of n-hexane-ethyl acetate, to obtain 240 mg of the desired product as colorless needles. Yield: 74%. m.p. 95-96° C.; [α]20D=−42.2° (C=0.386 AcOEt); MS(EI+) 323(M)+
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06429212B1 |
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| Source dataset | uspto-grants-2002_08 |
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| ORD ID | ord-292342b43bb24fccb9699e3fe7757c55 |
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| Source note | uspto-grants-2002_08 |
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