Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hexane | HCID 8058 | — |
| Reactant | Bis(tetrabutylammonium) sulphate | HCID 11433187 | — |
| Reactant | NaOH KH2PO4 | HCID 24942486 | — |
| Product | 2-Amino-5-(diethylamino)toluene | HCID 67364 | — |
Reaction Steps
In a 500-mL Parr® hydrogenation vessel, Compound CD-1 (8.74 g, 38 mmol) was dissolved in hexane (20 mL) and aqueous pH 7.4 buffer (20 mL; Fisher Scientific: SB110-1; potassium phosphate monobasic-sodium hydroxide buffer, 0.05 M). RhCl3.xH20 (1.0 g, 3.8 mmol; Alfa Aesar) and tetrabutylammonium sulfate solution (4.4 mL, 50 wt % in H2O; 4.4 g, 3.8 mmol) were added sequentially. The biphasic mixture was shaken under hydrogen atmosphere (53 psi) for 14 days at rt. The reaction mixture was filtered through a Celite® pad. The aq. layer was separated and extracted with EtOAc (3×15 mL). The combined organic layers was washed with brine (˜25 mL), dried over anhydrous MgSO4, filtered, and concentrated by rotary evaporation under reduced pressure. The crude product was purified by flash silica gel chromatography (Isco Combiflash Rf®; 80 g RediSep silica gel cartridge, 0-100% EtOAc/hexanes over 20 column volumes @ 80 mL/min). Eluent from column volumes 1-6, containing unreacted Compound CD-1, were discarded, while column volumes 7-20 were combined and concentrated to give desired product, Compound CD-2, as an off-white solid (6.67 g, 74% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08361959B2 |
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| Source dataset | uspto-grants-2013_01 |
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| ORD ID | ord-b7e87ef450574340b1a03f0072246d18 |
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| Source note | uspto-grants-2013_01 |
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