Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Isobutylamine | HCID 6558 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | 2,3,4,5-Tetrahydro-1-benzoxepine-8-carbaldehyde | HCID 57432274 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 60209724 | HCID 60209724 | 106.3% |
Reaction Steps
To a mixture of 0.48 g (2.7 mmol) of 2,3,4,5-tetrahydro-1-benzoxepine-8-carbaldehyde and 1.33 mL (13.5 mmol, 5 equiv) of isobutylamine in 22 mL of 1,2-dichloroethane was added 0.86 mL (15.0 mmol, 5.5 equiv) of acetic acid. The mixture was stirred under nitrogen at ambient temperature for 20 minutes and 0.64 g (3.0 mmol, 1.1 equiv) of sodium triacetoxyborohydride was added. The mixture was stirred overnight then diluted with 125 mL of ethyl acetate and washed with 60 mL each of saturated sodium bicarbonate solution, water and brine, dried over sodium sulfate, filtered, and concentrated under reduced pressure to give 0.67 g of a yellow oil. Purification by flash chromatography (0-10% methanol in ethyl acetate) gave the product as a colorless oil. MS (m+1)=234.2; 1H NMR (400 MHz, CDCl3) 7.07 (d, 1H, J 8 Hz), 7.09 (d, 1H, J 1.5 Hz), 6.99 (m, 1H), 3.99 (m, 2H), 3.72 (s, 2H), 2.70 (m, 2H), 2.43 (d, 2H, J 7 Hz), 1.95 (m, 2H), 1.77 (m, 1H), 1.71 (m, 2H), 1.5 (br s, 1H), 0.91 (d, 6H, J 7 Hz).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07855201B2 |
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| Source dataset | uspto-grants-2010_12 |
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| ORD ID | ord-22ed2c6a1ed4459683a0823216e232ff |
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| Source note | uspto-grants-2010_12 |
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