Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Acetylbiphenyl | HCID 7113 | — |
| Reactant | Glycine ethyl ester, hydrochloride | HCID 2723640 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Catalyst | Titanium isopropoxide | HCID 11026 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 43177456 | HCID 43177456 | 21.67% |
Reaction Steps
Titanium isopropoxide (4.4 g, 4.6 mL, and 15.5 mmol) was added to a stirred solution of 4-acetyl-biphenyl (1 g, 5.1 mmol) and glycine ethyl ester hydrochloride (2.2 g, 16.0 mmol) in MeOH (20 mL) and stirring continued at room temperature overnight. NaBH4 (800 mg, 20 mmol) was added in portion wise and the resulting mixture was stirred at room temperature for 10 hrs. The above mixture was quenched with 2N aqueous NH3 solution, filtered the solid precipitated. The filtrate was extracted with EtOAc, the organic layer was dried over Na2SO4 and concentrated under reduced pressure. The resulting residue was purified by column chromatography (using neutral alumina and 20% EtOAc in hexane as eluent) to afford 297 mg (21.67% yield) of (1-biphenyl-4-yl-ethylamino)-acetic acid methyl ester. 1H NMR (CDCl3): δ 7.64 (t, 4H), 7.5-7.3 (m, 5H), 3.9-3.8 (q, 2H), 3.7 (s, 3H), 3.4 (d, 2H), 1.5 (d, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07842696B2 |
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| Source dataset | uspto-grants-2010_11 |
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| ORD ID | ord-c2b53b6efac14048bf7091c128b94ae0 |
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| Source note | uspto-grants-2010_11 |
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