Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetaldehyde | HCID 177 | — |
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | HCID 131728472 | HCID 131728472 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 131728473 | HCID 131728473 | — |
Reaction Steps
Acetaldehyde (0.151 g, 3.4 mmol) was added to a solution of Example 92k (0.330 g, 0.68 mmol) in MeOH (10 mL) at 0° C. TFA (0.08 g, 0.68 mmol) was then added and stirring continued for 2 h. The reaction mixture was brought to room temperature, treated with sodium cyanoborohydride (0.108 g, 1.7 mmol) and allowed to stir for 4 h. It was concentrated, treated with aqueous sodium bicarbonate solution, water and extracted ethyl acetate. The organic layer was washed with water, brine, dried, concentrated and purified using flash chromatography to obtain the title compound. Yield: 0.80 g, (51%); 1H NMR (CDCl3): δ 1.20 (t, 2H, CH2), 1.70 (t, 2H, CH2), 1.80 (t, 4H, 2CH2), 2.70 (s, 3H, CH3), 2.80 (s, 2H, CH2), 2.90 (m, 2H, CH2), 3.40 (q, 2H, CH2), 3.80 (t, 2H, CH2), 3.9 (s, 3H, OCH3), 4.8 (s, 2H, CH2), 6.8 (s, 2H, Ar), 8.10 (s, 1H, Ar), 8.4 (s, 1H, Ar); MS: m/e (ES−) 506 (M−1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08183234B2 |
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| Source dataset | uspto-grants-2012_05 |
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| ORD ID | ord-7041da9a900c4f4db743bbdc6966cb38 |
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| Source note | uspto-grants-2012_05 |
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