HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium hydride → 4-Dodecyloxybenzyl(4-methoxymethyloxy-3-chlorophenyl) ether
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 3-Chloro-4-(methoxymethoxy)phenol | HCID 22221580 | — |
| Reactant | 1-(Bromomethyl)-4-(dodecyloxy)benzene | HCID 23052179 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-Dodecyloxybenzyl(4-methoxymethyloxy-3-chlorophenyl) ether | HCID 57105621 | 58.7% |
Reaction Steps
In dimethylformamide, 2 g of 4-dodecyloxybenzyl bromide synthesized in the same manner as described in Referential Example 17 was reacted with 1.5 g of 4-methoxymethyloxy-3-chlorophenol synthesized in the same manner as described in Example 11 in the presence of NaH to obtain 1.5 g of 4-dodecyloxybenzyl(4-methoxymethyloxy-3-chlorophenyl) ether. According to customary procedures, the methoxymethyl group was removed from the so-obtained compound in the presence of zinc in acetic acid to obtain 1.2 g of 4-dodecyloxybenzyl(4-hydroxy-3-chlorophenyl) ether.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04925591 |
| Source dataset | uspto-grants-1990_05 |
| ORD ID | ord-8a60b4385bf64dad8a53c453d3df97ef |
| Source note | uspto-grants-1990_05 |