HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,4-Butanediol → 4-(4-Acetyl-3-hydroxy-2-propylbenzyloxy)-1-butanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,4-Butanediol | HCID 8064 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 4-Acetyl-3-hydroxy-2-propylbenzyl chloride | HCID 13781022 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-(4-Acetyl-3-hydroxy-2-propylbenzyloxy)-1-butanol | HCID 15682684 | — |
Reaction Steps
To a suspension of 9.6 g. of a 50% oil dispersion of sodium hydride in 100 ml. of 1,4-butanediol were added 11.3 g. of 4-acetyl-3-hydroxy-2-propylbenzyl chloride. The reaction was stirred overnight at room temperature and then heated to 60° C. for six hours. The reaction mixture was then poured into water and extracted with ethyl acetate. The ethyl acetate solution was evaporated to dryness and the residue was purified by chromatography over silica gel to provide 14.1 g. of the desired title product. NMR.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05393768 |
| Source dataset | uspto-grants-1995_02 |
| ORD ID | ord-68c5ffadd61c4ec5a76950b5b0c3c717 |
| Source note | uspto-grants-1995_02 |