HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl 11-(p-tert-butylphenoxy)-undecanoate → 11-p-t-Butylphenoxy-1-undecanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl 11-(p-tert-butylphenoxy)-undecanoate | HCID 19797514 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 11-p-t-Butylphenoxy-1-undecanol | HCID 13313740 | — |
Reaction Steps
The methyl 11-(p-tert-butylphenoxy)-undecanoate, 3.7 g, 10.6 mmoles, was dissolved in 100 ml dry diethyl ether and added, dropwise, to a stirred slurry of 0.5 g lithium aluminum hydride in 100 ml dry diethyl ether. After one hour the reaction mixture was filtered through Celite and the filtrate was treated with 100 ml 1 N hydrochloric acid. The organic layer was removed, dried (MgSO4), and concentrated to a yellow oil, 2.7 g. The oil was chromatographed on 200 g 90 to 200 mesh silica gel (2% MeOH/CH2Cl2 eluent) collecting the product as a white, waxy solid. The solid was recrystallized from warm pentane yielding pure 11-(p-tert-butylphenoxy)-undecanol, 1.1 g, m.p. 39° to 40° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04451474 |
| Source dataset | uspto-grants-1984_05 |
| ORD ID | ord-667b857935554005b88bdb8daf9b0b70 |
| Source note | uspto-grants-1984_05 |