HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 2,2-Bis(6-benzyloxyhexyl)ethanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Ethyl 2,2-bis(6-benzyloxyhexyl)acetate | HCID 18920832 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 2,2-Bis(6-benzyloxyhexyl)ethanol | HCID 18920862 | 96% |
Reaction Steps
First, 0.44 g of lithium aluminium hydride and 50 ml of diethyl ether were placed in a 100 ml flask. Then, 5.4 g of ethyl 2,2-bis(6-benzyloxyhexyl)acetate obtained in Example 2-(d) was added dropwise to the reaction mixture under ice water cooling. The reaction mixture was stirred for 1 hour at room temperature and for 1 hour under reflux. The reaction mixture was poured into cold diluted hydrochloric acid. An ether layer was washed with water and dried over anhydrous sodium sulfate. Thereafter, the solvent was distilled away. The residue was purified by silica gel column chromatography (eluent: toluene/ethyl acetate=4/1) to obtain 4.7 g of 2,2-bis(6-benzyloxyhexyl)ethanol (Y: 96%). The compound thus obtained had a purity of 97.1% by GC.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05750213 |
| Source dataset | uspto-grants-1998_05 |
| ORD ID | ord-965c97fc7d054c17bad12ceeae3e9489 |
| Source note | uspto-grants-1998_05 |