HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → HCID 20230506, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | HCID 13565961 | HCID 13565961 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 20230506 | HCID 20230506 | 99.1% |
Reaction Steps
A mixture of 0.8 g of 1-(3,4-dibenzyloxyphenyl)-1,8-nonanedione and 10 ml of tetrahydrofuran was added to a solution of 0.1 g of lithium aluminum hydride in 50 ml of ether under ice-cooling followed by stirring for 2 hours at room temperature. Then, 50 ml of toluene was added to the reaction mixture and the mixture was acidified by the addition of diluted hydrochloric acid. The toluene layer was collected, washed with an aqueous 5% sodium hydrogencarbonate solution, washed with water, dried over anhydrous magnesium carbonate, and concentrated under reduced pressure to provide 0.8 g of 1-(3,4-dibenzyloxyphenyl)-1,8-nonanediol as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04618627 |
| Source dataset | uspto-grants-1986_10 |
| ORD ID | ord-88f955c65eb64a9393b9d0840df4c78e |
| Source note | uspto-grants-1986_10 |