Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 1-t-Butoxycarbonyl-4-trimethylstannyl-1,2,5,6-tetrahydropyridine | HCID 22022989 | — |
| Solvent | Ammonium Hydroxide | HCID 14923 | — |
| Product | HCID 86592233 | HCID 86592233 | 91% |
Reaction Steps
A modification of a procedure in the following reference herein incorporated by reference in its entirety, for all purposes as if fully set forth herein, was used: Boojamra, C. G.; Burow, K. M.; Thompson, L. A.; Ellman, J. A. J. Org. Chem., 1997, 62, 1240-1256. A solution of (NH4)2Fe(II)(SO4)2.6H2O (24.4 g, 63 mmol) in water (60 mL) was added to a stirred solution of 4-bromo-2-nitro-benzoic acid (2) (3.05 g, 12.45 mmol) in concentrated aqueous NH4OH (40 mL) at room temperature. The iron sulfate solution flask was washed with an additional portion of water (20 mL) which was added to the reaction. After 16 hours, the reaction had changed from a dark green solution to a rusty-brown mixture which was filtered through a plug of Celite and washed with concentrated aqueous NH4OH (80 mL) and water (4×80 mL). The combined aqueous fractions were acidified to pH 1-2 with aqueous concentrated HCl and extracted with EtOAc (4×500 mL). The organic fractions were evaporated under reduced pressure to a brown solid. The crude product was dissolved in EtOAc (300 mL), washed with water (40 mL), brine (40 mL), dried with Na2SO4, filtered, and concentrated to dryness giving 2.47 g of product (3) as a brown solid in 91% yield and >90% purity by HPLC.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07825132B2 |
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| Source dataset | uspto-grants-2010_11 |
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| ORD ID | ord-cafd8b3604c4492d94998be1d5a37896 |
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| Source note | uspto-grants-2010_11 |
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