HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Dodecyloxy-2-chlorobenzoic acid → 4-Dodecyloxy-2-chlorobenzyl alcohol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Dodecyloxy-2-chlorobenzoic acid | HCID 19738841 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Product | 4-Dodecyloxy-2-chlorobenzyl alcohol | HCID 54388926 | — |
Reaction Steps
According to customary procedures, 4-dodecyloxy-2-chlorobenzoic acid synthesized in the same manner as described in Referential Example 15 was reduced with LiAlH4 to obtain 4-dodecyloxy-2-chlorobenzyl alcohol, and this compound was brominated with PBr3 to obtain 4-dodecyloxy-2-chlorobenzyl bromide. In the same manner as described in Referential Example 18, 2.0 g of the so-obtained compound was reacted with 1.0 g of 4-acetoxyphenol to obtain 4-dodecyloxy-2-chlorobenzyl(4-acetoxyphenyl) ether. Then, the acetyl group was removed by an equimolar amount of LiOH, whereby 0.9 g of 4-dodecyloxy-2-chlorobenzyl(4-hydroxyphenyl) ether was obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04925591 |
| Source dataset | uspto-grants-1990_05 |
| ORD ID | ord-37132dbda6bf422f8118ed0261d86571 |
| Source note | uspto-grants-1990_05 |