Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 58707339 | HCID 58707339 | — |
| Catalyst | Titanium isopropoxide | HCID 11026 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 58707283 | HCID 58707283 | 89% |
Reaction Steps
To a stirred solution of 1-(5-fluoro-2-methoxy-3-chlorophenyl)ethanone (1.9 g, 9.38 mmol), titanium(IV) isopropoxide (5.54 mL, 18.76 mmol) and ammonia in ethanol (23.5 mL) was stirred under nitrogen in a capped flask at ambient temperature for 6 h. Sodium borohydride (0.53 g, 14.07 mmol) was added and resulting mixture was stirred at room temperature for 3 h. The reaction was then quenched by pouring into ammonium hydroxide (40 mL), the resulting inorganic precipitate was filtered off, and washed with ethyl acetate (2×40 mL). the organic layer was separated and aqueous layer was extracted with ethyl acetate (2×40 mL). The combined organic layers were dried over Na2SO4, filtered, and evaporated to afford 1-(5-Fluoro-2-methoxy-3-chlorophenyl)ethanamine (1.7 g, 89%): 1H NMR (400 MHz, CDCl3): δ 6.78 (dd, 1H), 6.68 (dd, 1H), 4.25 (m, 1H), 3.82 (s, 3H), 1.42 (d, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08604021B2 |
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| Source dataset | uspto-grants-2013_12 |
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| ORD ID | ord-8dd23aec9a54403e95630701ed58f2eb |
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| Source note | uspto-grants-2013_12 |
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