Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzocaine | HCID 2337 | — |
| Reactant | Isobutylene | HCID 8255 | — |
| Reactant | 3-(Methylsulfonyl)benzaldehyde | HCID 13596602 | — |
| Reactant | Ytterbium(3+) trifluoromethanesulfonate--water (1/3/1) | HCID 45075687 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 70496554 | HCID 70496554 | 43% |
Reaction Steps
A mixture of 4-aminobenzoic acid ethyl ester (3.3 g, 20 mmol), 3-methanesulfonyl benzaldehyde (3.68 g, 20 mmol) and ytterbium(III) triflate hydrate (1.86 g, 3 mmol) in acetonitrile (150 mL) was cooled to 0° C. in a sealed reaction bottle. Then a cooled solution of isobutene (5.6 g, 100 mmol) was added into. The reaction mixture was heated to 90° C. and stirred for 12 h. The solvent was removed in vacuo and the residue was purified on flash silica gel chromatography (silica gel from QingDao, 200-300 mesh, glass column from Shanghai SD company) (10% ethyl acetate/hexanes) to afford 2-(3-methanesulfonyl-phenyl)-4,4-dimethyl-1,2,3,4-tetrahydro-quinoline-6-carboxylic acid ethyl ester (3.3 g, 43%) as a white solid: MS (ESI) M+1=388.3.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08809369B2 |
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| Source dataset | uspto-grants-2014_08 |
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| ORD ID | ord-30ae4b92a0bb4693abd615872e4f8ead |
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| Source note | uspto-grants-2014_08 |
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