HuagongsheHuagongshe Chemistry Print Report · For research reference only
(+-)-4-Hydroxymandelic acid → p-Nitrobenzyl 4-hydroxymandelate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (+-)-4-Hydroxymandelic acid | HCID 328 | — |
| Reactant | Dimethylacetamide | HCID 31374 | — |
| Reactant | 4-Nitrobenzyl bromide | HCID 66011 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | p-Nitrobenzyl 4-hydroxymandelate | HCID 13066460 | 84% |
Reaction Steps
To a solution of 16.8 g. (0.1 mole) of 4-hydroxymandelic acid in 300 ml. of dimethylacetamide were added 11.2 g. of potassium t-butoxide with an additional 100 ml. of dimethylacetamide. The mixture was stirred at room temperature until a solution was obtained. p-Nitrobenzyl bromide (21.6 g., 0.1 mole) was added to the solution followed by 100 ml. of additional dimethylacetamide. The reaction mixture was stirred for 24 hours and was diluted with one liter of ethyl acetate. The mixture was washed repeatedly with water and dried over magnesium sulfate. The dried solution was evaporated to yield 25 g. (84 percent yield) of p-nitrobenzyl 4-hydroxymandelate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04355172 |
| Source dataset | uspto-grants-1982_10 |
| ORD ID | ord-97b1b52820544c818657c0ef02c23237 |
| Source note | uspto-grants-1982_10 |