HuagongsheHuagongshe Chemistry Print Report · For research reference only
Formaldehyde → HCID 178483491, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | HCID 178453920 | HCID 178453920 | — |
| Catalyst | Acetic Acid | HCID 176 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Sodium Bicarbonate | HCID 516892 | — |
| Product | HCID 178483491 | HCID 178483491 | 31.1% |
Reaction Steps
To a suspension of tert-butyl (trans-4-(2-aminoethyl)cyclohexyl)carbamate (970 mg, 4 mmol) and paraformaldehyde (360 mg, 12 mmol) in methanol (40 mL) was added sodium cyanoborohydride (754 mg, 12 mmol) and acetic acid (1 drop). The resultant suspension was stirred at room temperature for 16 h, diluted with a saturated NaHCO3 solution and extracted with a mixture of CHCl3/isopropanol (3:1). The combined organic layers were dried over anhydrous sodium sulfate and concentrated. Purification by column chromatography (silica, 0-20% methanol/dichloromethane) afforded the desired product (336 mg, 31%) as a white solid. ESI MS m/z 271 [C15H30N2O2+H]+
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09120749B2 |
| Source dataset | uspto-grants-2015_09 |
| ORD ID | ord-32f3accd48774fc58d8d88595df099fb |
| Source note | uspto-grants-2015_09 |