HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Hydroxide → 3-Hept-4-ylamino-8-t-butyl-1-oxaspiro(4,5)-decane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 4-Heptanone | HCID 31246 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | 3-Amino-8-t-butyl-1-oxaspiro(4,5)-decane | HCID 19040163 | — |
| Catalyst | Zincchloride | HCID 3007855 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 3-Hept-4-ylamino-8-t-butyl-1-oxaspiro(4,5)-decane | HCID 19040152 | 72.4% |
Reaction Steps
To 3-amino-8-t-butyl-1-oxaspiro(4,5)-decane (1.12 g, 5 mmol) and heptane-4-one (0.6 g, 5.25 mmol) in dry methanol (20 ml) was added zinc chloride (0.41 g, 3 mmol). The mixture was stirred at room temperature for 5 minutes and sodium cyanoborohydride 0.38 g, 6 mmol) was added and the resulting heterogeneous mixture was stirred at room temperature overnight. The solvent was then stripped off in vacuo, toluene (50 ml) and 2N NaOH (50 ml) was added. The aqueous phase was extracted twice with toluene (2×50 ml) and the combined organic layers were dried (MgSO4) and concentrated in vacuo. The resulting oil was purified by flash chromatography to give a pale yellow oil (1.12 g). nD :1.4726.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05641883 |
| Source dataset | uspto-grants-1997_06 |
| ORD ID | ord-adc1bce63f7640a5b9e533a0d2e65894 |
| Source note | uspto-grants-1997_06 |