HuagongsheHuagongshe Chemistry Print Report · For research reference only
Chlorohydroquinone → 4-Dodecyloxybenzyl(4-hydroxy-2-chlorophenyl) ether
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Chlorohydroquinone | HCID 301 | — |
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 1-(Bromomethyl)-4-(dodecyloxy)benzene | HCID 23052179 | — |
| Product | 4-Dodecyloxybenzyl(4-hydroxy-2-chlorophenyl) ether | HCID 56975878 | — |
Reaction Steps
In an aqueous solution of sodium hydroxide, 2.0 g of 4-dodecyloxybenzyl bromide synthesized in the same manner as described in Referential Example 17 was reacted under reflux with 1.0 g of 4-hydroxy-3-chlorophenol for 8 hours, the thus-obtained solution was put into ice-cooled hydrochloric acid, and the precipitate was recovered by filtration, washed, dried and purified by the silica gel column chromatography to obtain 0.8 g of 4-dodecyloxybenzyl(4-hydroxy-2-chlorophenyl) ether.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04925591 |
| Source dataset | uspto-grants-1990_05 |
| ORD ID | ord-01eaf141db0c4242a015161c5ff95c91 |
| Source note | uspto-grants-1990_05 |