HuagongsheHuagongshe Chemistry Print Report · For research reference only
Butanal → HCID 12967662, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Butanal | HCID 261 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Sulfuric acid magnesium salt (1:1) | HCID 24083 | — |
| Reactant | Leucine methyl ester hydrochloride | HCID 2723695 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 12967662 | HCID 12967662 | 27.1% |
Reaction Steps
Synthesized according to the general procedure as described in Example 1a using L-leucine methyl ester hydrochloride (1.5 gm, 8.25 mmol), THF (25 mL), MgSO4 (1.68 gm, 14.02 mmol), butyraldehyde (1.45 mL, 16.5 mmol), Et3N (1.14 mL, 8.25 mmol), sodium borohydride (625 mg, 16.5 mmol), and methanol (25 mL) to give 11j (450 mg, 27%) in FIG. 2. 1H NMR (500 MHz, CDCl3): δ 0.86-0.98 (9H, m), 1.24-1.52 (7H, m), 1.64-1.74 (1H, heptet), 2.4-2.48 (1H, m), 2.52-2.6 (1H, m), 3.27 (1H, t, J=7.33 Hz), 3.71 (3H, s). ESI-MS: 224.1 (M+23).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08552208B2 |
| Source dataset | uspto-grants-2013_10 |
| ORD ID | ord-21e6037be1e9449c84e2449be8444e48 |
| Source note | uspto-grants-2013_10 |