HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → HCID 13076850, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | 1-(5-Cyclohexyl-2-hydroxyphenyl)ethan-1-one | HCID 13076842 | — |
| Reactant | HCID 178418255 | HCID 178418255 | — |
| Product | HCID 13076850 | HCID 13076850 | — |
Reaction Steps
310 ml of an ether solution titrating 0.76 M/liter of phenyl magnesium bromide were added over 1 hour to a mixture of 23.4 g of the product of Step A and 230 ml of anhydrous ether and the mixture was stirred for 16 hours at room temperature and was poured over ice. The mixture was acidified with 200 ml of 2 N hydrochloric acid and was extracted 3 times with 250 ml of ether. The organic phase was washed 3 times with 100 ml of water, dried over magnesium sulfate and evaporated to dryness under reduced pressure. The residue was taken up in 120 ml of petroleum ether (b.p.=60° to 80° C.) and the mixture was vacuum filtered. The product was dried to obtain 22.55 g of 5-cyclohexyl-2-hydroxy-α-methyl-α-phenyl-benzene-methanol melting at 119° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04281012 |
| Source dataset | uspto-grants-1981_07 |
| ORD ID | ord-67c71698d676457f9af9162f9303608b |
| Source note | uspto-grants-1981_07 |