HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diethyl Ether → Tert-butyl 4-(2-hydroxyethyl)benzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Tert-butyl 4-formylbenzoate | HCID 2751588 | — |
| Reactant | HCID 178418573 | HCID 178418573 | — |
| Product | Tert-butyl 4-(2-hydroxyethyl)benzoate | HCID 10331132 | — |
Reaction Steps
t-Butyl p-formylbenzoate (20 g, 97 mmol) was dissolved in dry diethyl ether (300 ml), followed by the dropwise addition of methylmagnesium bromide ethereal solution, 33 ml) under cooling with ice and stirring. The obtained mixture was stirred for one hour and poured into a saturated aqueous solution of ammonium chloride, and the obtained mixture was extracted with ether. The ethereal phase was washed with water, dried and distilled to remove the solvent. The pale-yellow viscous liquid residue thus obtained was subjected to silica gel column chromatography and eluted with a solvent (ethyl acetate/hexane=1:4) to give 21.8 g of t-butyl 4-(hydroxyethyl)benzoate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05688800 |
| Source dataset | uspto-grants-1997_11 |
| ORD ID | ord-3a7b139cf162448587560a6416e2f17c |
| Source note | uspto-grants-1997_11 |