HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → 1-Acetylamino-11-benzyloxy-1,1-diethoxycarbonylundecane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Reactant | 1-Benzyloxy-10-iododecane | HCID 13712769 | — |
| Reactant | Diethyl acetamide malonate | HCID 22466969 | — |
| Product | 1-Acetylamino-11-benzyloxy-1,1-diethoxycarbonylundecane | HCID 22467011 | 89.7% |
Reaction Steps
Anhydrous ethanol (10.5 ml) and diethylacetamide malonate (2661 mg, 12.25 mmols) were added to sodium ethoxide (834 mg, 12.25 mmols). After stirring for 10 minutes, 1-benzyloxy-10-iododecane (Compound q-1) (2661 mg, 12.25 mmols) was added to the mixture. The mixture was heated to reflux for 4 hours and concentrated in vacuo. Chloroform (200 ml) and water (100 ml) were added to the residue for separation. The organic layer was washed with saturated sodium chloride aqueous solution (100 ml), dried over anhydrous sodium sulfate and then concentrated. The residue was purified by silica gel column chromatography (300 ml, hexane:ethyl acetate=4:1) to give Compound (r-2) (5080 mg, yield: 89.7%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06384063B1 |
| Source dataset | uspto-grants-2002_05 |
| ORD ID | ord-78d2e175a8964d72bbfa64e91fb6ac82 |
| Source note | uspto-grants-2002_05 |