Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Benzenamine, 4-(phenylmethyl)- | HCID 136914 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | N-(tert-Butoxycarbonyl)-D-prolinal | HCID 7009153 | — |
| Solvent | 1,1-Dichloroethane | HCID 6365 | — |
| Solvent | Sodium Bicarbonate | HCID 516892 | — |
| Product | HCID 68998869 | HCID 68998869 | 85% |
Reaction Steps
To a solution of 4-benzyl aniline (200 mg, 1.1 mmol) in dichloroethane (1.5 mL) was added a solution of N-(t-butoxycarbonyl)-D-prolinal (239 mg, 1.2 mmol) in dichloroethane (1.5 mL) at 0-5° C. Sodium triacetoxyborohydride (393 mg, 1.85 mmol) was added to the above solution. Acetic acid (65 mg, 1.1 mmol) in dichloroethane (1 mL) was added dropwise, over a period of 5 min at 0-5° C. The reaction mixture was stirred at 0-10° C. for 3 h. The mixture was diluted with saturated aq NaHCO3 and extracted with dichoromethane. Organic layer was dried over anhy. MgSO4 and the solvent was removed in vacuo to obtain the crude mixture, which was purified by silica gel flash chromatography to obtain the title product (340 mg, 85%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08598359B2 |
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| Source dataset | uspto-grants-2013_12 |
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| ORD ID | ord-dcc6aed7cb29449bb0b06a3dc2bfa3a5 |
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| Source note | uspto-grants-2013_12 |
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